Details for New Drug Application (NDA): 207783
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The generic ingredient in CYPROHEPTADINE HYDROCHLORIDE is cyproheptadine hydrochloride. There are six drug master file entries for this compound. Twenty-three suppliers are listed for this compound. Additional details are available on the cyproheptadine hydrochloride profile page.
Summary for 207783
Tradename: | CYPROHEPTADINE HYDROCHLORIDE |
Applicant: | Rising |
Ingredient: | cyproheptadine hydrochloride |
Patents: | 0 |
Formulation / Manufacturing: | see details |
Medical Subject Heading (MeSH) Categories for 207783
Suppliers and Packaging for NDA: 207783
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
CYPROHEPTADINE HYDROCHLORIDE | cyproheptadine hydrochloride | TABLET;ORAL | 207783 | ANDA | Proficient Rx LP | 71205-024 | 71205-024-30 | 30 TABLET in 1 BOTTLE, PLASTIC (71205-024-30) |
CYPROHEPTADINE HYDROCHLORIDE | cyproheptadine hydrochloride | TABLET;ORAL | 207783 | ANDA | Proficient Rx LP | 71205-024 | 71205-024-60 | 60 TABLET in 1 BOTTLE, PLASTIC (71205-024-60) |
Profile for product number 001
Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 4MG | ||||
Approval Date: | Dec 29, 2016 | TE: | RLD: | No |
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