Details for New Drug Application (NDA): 040466
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The generic ingredient in DIPHENHYDRAMINE HYDROCHLORIDE is diphenhydramine hydrochloride. There are twenty-three drug master file entries for this compound. Eighteen suppliers are listed for this compound. Additional details are available on the diphenhydramine hydrochloride profile page.
Summary for 040466
| Tradename: | DIPHENHYDRAMINE HYDROCHLORIDE |
| Applicant: | App Pharms |
| Ingredient: | diphenhydramine hydrochloride |
| Patents: | 0 |
Pharmacology for NDA: 040466
| Mechanism of Action | Histamine H1 Receptor Antagonists |
Medical Subject Heading (MeSH) Categories for 040466
Suppliers and Packaging for NDA: 040466
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| DIPHENHYDRAMINE HYDROCHLORIDE | diphenhydramine hydrochloride | INJECTABLE;INJECTION | 040466 | ANDA | HF Acquisition Co LLC, DBA HealthFirst | 51662-1348 | 51662-1348-1 | 1 mL in 1 VIAL (51662-1348-1) |
| DIPHENHYDRAMINE HYDROCHLORIDE | diphenhydramine hydrochloride | INJECTABLE;INJECTION | 040466 | ANDA | HF Acquisition Co LLC, DBA HealthFirst | 51662-1374 | 51662-1374-1 | 1 mL in 1 VIAL, SINGLE-DOSE (51662-1374-1) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 50MG/ML | ||||
| Approval Date: | May 28, 2002 | TE: | AP | RLD: | No | ||||
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