Details for New Drug Application (NDA): 206553
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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 206553
Tradename: | CYPROHEPTADINE HYDROCHLORIDE |
Applicant: | Appco |
Ingredient: | cyproheptadine hydrochloride |
Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 206553
Suppliers and Packaging for NDA: 206553
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
CYPROHEPTADINE HYDROCHLORIDE | cyproheptadine hydrochloride | TABLET;ORAL | 206553 | ANDA | QPharma Inc | 42708-177 | 42708-177-21 | 21 TABLET in 1 BOTTLE, PLASTIC (42708-177-21) |
CYPROHEPTADINE HYDROCHLORIDE | cyproheptadine hydrochloride | TABLET;ORAL | 206553 | ANDA | A-S Medication Solutions | 50090-5491 | 50090-5491-1 | 30 TABLET in 1 BOTTLE (50090-5491-1) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 4MG | ||||
Approval Date: | Nov 29, 2016 | TE: | AA | RLD: | No |
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