CYPROHEPTADINE HYDROCHLORIDE
- Product NDC
- 63629-2062
- 11-digit product format
- 636292062
- Labeler code
- 63629
- Product ID
- 63629-2062_1eabc797-74c9-4872-b680-7aecee22294e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CYPROHEPTADINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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 |
|---|
| 63629-2062-1 | 63629206201 | 1000 TABLET in 1 BOTTLE (63629-2062-1) | 1000 tablet | 2013-10-21 | 2023-02-28 | No | No | Current |