Cyproheptadine Hydrochloride
- Product NDC
- 64720-150
- 11-digit product format
- 647200150
- Labeler code
- 64720
- Product ID
- 64720-150_9ae6858a-9bee-4010-963e-a98f64c157ca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyproheptadine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- CorePharma, LLC
- Application
- ANDA040537
- Marketing category
- ANDA
- Marketing start
- 2015-07-29
- Marketing end
- 2020-02-01
- Substance
- CYPROHEPTADINE HYDROCHLORIDE
- Active strength
- 4 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record