CYPROHEPTADINE HYDROCHLORIDE
- Product NDC
- 71335-2964
- 11-digit product format
- 713352964
- Labeler code
- 71335
- Product ID
- 71335-2964_ccf448d1-4daf-4db0-9134-6ea5bf0409eb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CYPROHEPTADINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA212491
- Marketing category
- ANDA
- Marketing start
- 2021-02-24
- Substance
- CYPROHEPTADINE HYDROCHLORIDE
- Active strength
- 4 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| NJ82J0F8QC | CYPROHEPTADINE HYDROCHLORIDE | 41354-29-4 | CYPROHEPTADINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2964-1 | 71335296401 | 90 TABLET in 1 BOTTLE (71335-2964-1) | 90 tablet | 2025-11-10 | No | No | Historical |