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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- CYPROHEPTADINE HYDROCHLORIDE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CYPROHEPTADINE HYDROCHLORIDE | 4 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | NJ82J0F8QC |
| Rxcui | 866144 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-2964-1 | CYPROHEPTADINE HYDROCHLORIDE | 90 in 1 BOTTLE | TABLET | 90 | | 100 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| 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 | Current |