List of Excipients in API fexofenadine hydrochloride oral
✉ Email this page to a colleague
Excipients in ANDA-approved (generic) drugs containing fexofenadine hydrochloride oral
| Company | Ingredient | NDC | Excipient |
|---|---|---|---|
| Aurohealth LLC | fexofenadine hydrochloride oral | 58602-426 | EDETATE DISODIUM |
| Aurohealth LLC | fexofenadine hydrochloride oral | 58602-426 | ETHYLPARABEN |
| Aurohealth LLC | fexofenadine hydrochloride oral | 58602-426 | METHYLPARABEN |
| >Company | >Ingredient | >NDC | >Excipient |
Detailed excipient profiles for fexofenadine hydrochloride oral
Excipient focus: EDETATE DISODIUM
fexofenadine hydrochloride oral drug variants containing EDETATE DISODIUM
| Company | Ingredient | NDC |
|---|---|---|
| Aurohealth LLC | fexofenadine hydrochloride oral | 58602-426 |
| >Company | >Ingredient | >NDC |
fexofenadine hydrochloride oral drug variants not containing EDETATE DISODIUM
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: ETHYLPARABEN
fexofenadine hydrochloride oral drug variants containing ETHYLPARABEN
| Company | Ingredient | NDC |
|---|---|---|
| Aurohealth LLC | fexofenadine hydrochloride oral | 58602-426 |
| >Company | >Ingredient | >NDC |
fexofenadine hydrochloride oral drug variants not containing ETHYLPARABEN
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: METHYLPARABEN
fexofenadine hydrochloride oral drug variants containing METHYLPARABEN
| Company | Ingredient | NDC |
|---|---|---|
| Aurohealth LLC | fexofenadine hydrochloride oral | 58602-426 |
| >Company | >Ingredient | >NDC |
fexofenadine hydrochloride oral drug variants not containing METHYLPARABEN
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: MODIFIED CORN STARCH
fexofenadine hydrochloride oral drug variants containing MODIFIED CORN STARCH
| Company | Ingredient | NDC |
|---|---|---|
| Aurohealth LLC | fexofenadine hydrochloride oral | 58602-426 |
| >Company | >Ingredient | >NDC |
fexofenadine hydrochloride oral drug variants not containing MODIFIED CORN STARCH
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: POLOXAMER 407
fexofenadine hydrochloride oral drug variants containing POLOXAMER 407
| Company | Ingredient | NDC |
|---|---|---|
| Aurohealth LLC | fexofenadine hydrochloride oral | 58602-426 |
| >Company | >Ingredient | >NDC |
fexofenadine hydrochloride oral drug variants not containing POLOXAMER 407
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: PROPYLENE GLYCOL
fexofenadine hydrochloride oral drug variants containing PROPYLENE GLYCOL
| Company | Ingredient | NDC |
|---|---|---|
| Aurohealth LLC | fexofenadine hydrochloride oral | 58602-426 |
| >Company | >Ingredient | >NDC |
fexofenadine hydrochloride oral drug variants not containing PROPYLENE GLYCOL
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: SODIUM PHOSPHATE, DIBASIC, ANHYDROUS
fexofenadine hydrochloride oral drug variants containing SODIUM PHOSPHATE, DIBASIC, ANHYDROUS
| Company | Ingredient | NDC |
|---|---|---|
| Aurohealth LLC | fexofenadine hydrochloride oral | 58602-426 |
| >Company | >Ingredient | >NDC |
fexofenadine hydrochloride oral drug variants not containing SODIUM PHOSPHATE, DIBASIC, ANHYDROUS
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
fexofenadine hydrochloride oral drug variants containing SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
| Company | Ingredient | NDC |
|---|---|---|
| Aurohealth LLC | fexofenadine hydrochloride oral | 58602-426 |
| >Company | >Ingredient | >NDC |
fexofenadine hydrochloride oral drug variants not containing SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: STRAWBERRY
fexofenadine hydrochloride oral drug variants containing STRAWBERRY
| Company | Ingredient | NDC |
|---|---|---|
| Aurohealth LLC | fexofenadine hydrochloride oral | 58602-426 |
| >Company | >Ingredient | >NDC |
fexofenadine hydrochloride oral drug variants not containing STRAWBERRY
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: SUCROSE
fexofenadine hydrochloride oral drug variants containing SUCROSE
| Company | Ingredient | NDC |
|---|---|---|
| Aurohealth LLC | fexofenadine hydrochloride oral | 58602-426 |
| >Company | >Ingredient | >NDC |
fexofenadine hydrochloride oral drug variants not containing SUCROSE
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: TITANIUM DIOXIDE
fexofenadine hydrochloride oral drug variants containing TITANIUM DIOXIDE
| Company | Ingredient | NDC |
|---|---|---|
| Aurohealth LLC | fexofenadine hydrochloride oral | 58602-426 |
| >Company | >Ingredient | >NDC |
fexofenadine hydrochloride oral drug variants not containing TITANIUM DIOXIDE
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: TRIACETIN
fexofenadine hydrochloride oral drug variants containing TRIACETIN
| Company | Ingredient | NDC |
|---|---|---|
| Aurohealth LLC | fexofenadine hydrochloride oral | 58602-426 |
| >Company | >Ingredient | >NDC |
fexofenadine hydrochloride oral drug variants not containing TRIACETIN
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: WATER
fexofenadine hydrochloride oral drug variants containing WATER
| Company | Ingredient | NDC |
|---|---|---|
| Aurohealth LLC | fexofenadine hydrochloride oral | 58602-426 |
| >Company | >Ingredient | >NDC |
fexofenadine hydrochloride oral drug variants not containing WATER
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: XANTHAN GUM
fexofenadine hydrochloride oral drug variants containing XANTHAN GUM
| Company | Ingredient | NDC |
|---|---|---|
| Aurohealth LLC | fexofenadine hydrochloride oral | 58602-426 |
| >Company | >Ingredient | >NDC |
fexofenadine hydrochloride oral drug variants not containing XANTHAN GUM
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: XYLITOL
fexofenadine hydrochloride oral drug variants containing XYLITOL
| Company | Ingredient | NDC |
|---|---|---|
| Aurohealth LLC | fexofenadine hydrochloride oral | 58602-426 |
| >Company | >Ingredient | >NDC |
fexofenadine hydrochloride oral drug variants not containing XYLITOL
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Make Better Decisions: Try a trial or see plans & pricing
Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.
