Cyproheptadine Hydrochloride
- Product NDC
- 24689-816
- 11-digit product format
- 246890816
- Labeler code
- 24689
- Product ID
- 24689-816_e584b51e-ff2d-52c5-e053-2995a90a8201
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyproheptadine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Apnar Pharma
- Application
- ANDA207555
- Marketing category
- ANDA
- Marketing start
- 2018-05-15
- Marketing end
- 2023-02-28
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 24689-816-01 | 24689081601 | 100 TABLET in 1 BOTTLE (24689-816-01) | 100 tablet | 2018-05-21 | 0000-00-00 | No | No | Current |
| 24689-816-10 | 24689081610 | 1000 TABLET in 1 BOTTLE (24689-816-10) | 1000 tablet | 2018-05-21 | 0000-00-00 | No | No | Current |