CYPROHEPTADINE HYDROCHLORIDE
- Product NDC
- 70518-1886
- 11-digit product format
- 705181886
- Labeler code
- 70518
- Product ID
- 70518-1886_82837451-6d81-2197-e053-2991aa0aa80a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CYPROHEPTADINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA205087
- Marketing category
- ANDA
- Marketing start
- 2019-02-20
- Marketing end
- 0000-00-00
- Substance
- CYPROHEPTADINE HYDROCHLORIDE
- Active strength
- 4 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record