Details for New Drug Application (NDA): 088212
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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 088212
Tradename: | CYPROHEPTADINE HYDROCHLORIDE |
Applicant: | Chartwell Rx |
Ingredient: | cyproheptadine hydrochloride |
Patents: | 0 |
Formulation / Manufacturing: | see details |
Medical Subject Heading (MeSH) Categories for 088212
Suppliers and Packaging for NDA: 088212
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
CYPROHEPTADINE HYDROCHLORIDE | cyproheptadine hydrochloride | TABLET;ORAL | 088212 | ANDA | Chartwell RX, LLC | 62135-236 | 62135-236-90 | 90 TABLET in 1 BOTTLE (62135-236-90) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 4MG | ||||
Approval Date: | May 26, 1983 | TE: | AA | RLD: | No |
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