CYPROHEPTADINE HYDROCHLORIDE
- Product NDC
- 50488-5002
- 11-digit product format
- 504885002
- Labeler code
- 50488
- Product ID
- 50488-5002_c968511a-6976-451a-8976-47c332d60495
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CYPROHEPTADINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Alexso, Inc
- Application
- ANDA205087
- Marketing category
- ANDA
- Marketing start
- 2015-09-23
- Marketing end
- 0000-00-00
- Substance
- CYPROHEPTADINE HYDROCHLORIDE
- Active strength
- 4 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50488-5002-1 | 50488500201 | 100 TABLET in 1 BOTTLE, PLASTIC (50488-5002-1) | 100 tablet | 2015-09-23 | 0000-00-00 | No | No | Current |
| 50488-5002-2 | 50488500202 | 1000 TABLET in 1 BOTTLE, PLASTIC (50488-5002-2) | 1000 tablet | 2015-09-23 | 0000-00-00 | No | No | Current |