Cyproheptadine Hydrochloride
- Product NDC
- 71335-2368
- 11-digit product format
- 713352368
- Labeler code
- 71335
- Product ID
- 71335-2368_e672afab-de82-4aa0-9d12-f1d7d21dc6c7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyproheptadine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040537
- Marketing category
- ANDA
- Marketing start
- 2015-07-29
- 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 |
|---|
| 71335-2368-1 | 71335236801 | 30 TABLET in 1 BOTTLE (71335-2368-1) | 30 tablet | 2024-05-23 | No | No | Historical |
| 71335-2368-2 | 71335236802 | 60 TABLET in 1 BOTTLE (71335-2368-2) | 60 tablet | 2024-05-23 | No | No | Historical |
| 71335-2368-3 | 71335236803 | 28 TABLET in 1 BOTTLE (71335-2368-3) | 28 tablet | 2024-05-23 | No | No | Historical |
| 71335-2368-4 | 71335236804 | 100 TABLET in 1 BOTTLE (71335-2368-4) | 100 tablet | 2024-05-23 | No | No | Historical |
| 71335-2368-5 | 71335236805 | 90 TABLET in 1 BOTTLE (71335-2368-5) | 90 tablet | 2024-05-23 | No | No | Historical |