CYPROHEPTADINE HYDROCHLORIDE
- Product NDC
- 51991-838
- 11-digit product format
- 519910838
- Labeler code
- 51991
- Product ID
- 51991-838_bafb4a6b-b611-47d0-9e58-ccbd9f2676da
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CYPROHEPTADINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Breckenridge Pharmaceutical, Inc.
- Application
- ANDA040644
- Marketing category
- ANDA
- Marketing start
- 2013-10-21
- Marketing end
- 2024-01-31
- 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 |
|---|
| 51991-838-01 | 51991083801 | 100 TABLET in 1 BOTTLE (51991-838-01) | 100 tablet | 2013-10-21 | 0000-00-00 | No | No | Current |
| 51991-838-10 | 51991083810 | 1000 TABLET in 1 BOTTLE (51991-838-10) | 1000 tablet | 2013-10-21 | 2023-02-28 | No | No | Current |