Details for New Drug Application (NDA): 208938
✉ Email this page to a colleague
The generic ingredient in CYPROHEPTADINE HYDROCHLORIDE is cyproheptadine hydrochloride. There are six drug master file entries for this compound. Twenty-two suppliers are listed for this compound. Additional details are available on the cyproheptadine hydrochloride profile page.
Summary for 208938
Tradename: | CYPROHEPTADINE HYDROCHLORIDE |
Applicant: | Zydus Pharms |
Ingredient: | cyproheptadine hydrochloride |
Patents: | 0 |
Formulation / Manufacturing: | see details |
Medical Subject Heading (MeSH) Categories for 208938
Suppliers and Packaging for NDA: 208938
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
CYPROHEPTADINE HYDROCHLORIDE | cyproheptadine hydrochloride | TABLET;ORAL | 208938 | ANDA | A-S Medication Solutions | 50090-6129 | 50090-6129-1 | 30 TABLET in 1 BOTTLE (50090-6129-1) |
CYPROHEPTADINE HYDROCHLORIDE | cyproheptadine hydrochloride | TABLET;ORAL | 208938 | ANDA | Zydus Pharmaceuticals USA Inc. | 70710-1110 | 70710-1110-0 | 1000 TABLET in 1 BOTTLE (70710-1110-0) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 4MG | ||||
Approval Date: | May 19, 2017 | TE: | AA | RLD: | No |
Complete Access Available with Subscription