Cyproheptadine Hydrochloride
- Product NDC
- 13811-694
- 11-digit product format
- 138110694
- Labeler code
- 13811
- Product ID
- 13811-694_5cd0a23f-b65e-46a8-9394-0d6296c40ca1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyproheptadine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Trigen Laboratories
- Application
- ANDA207555
- Marketing category
- ANDA
- Marketing start
- 2017-02-22
- Marketing end
- 0000-00-00
- Substance
- CYPROHEPTADINE HYDROCHLORIDE
- Active strength
- 4 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record