Cyproheptadine Hydrochloride
- Product NDC
- 62135-236
- 11-digit product format
- 621350236
- Labeler code
- 62135
- Product ID
- 62135-236_f33fcf42-0b48-eed9-e053-2995a90abefb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyproheptadine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Chartwell RX, LLC
- Application
- ANDA088212
- Marketing category
- ANDA
- Marketing start
- 1983-05-26
- 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 |
|---|
| 62135-236-90 | Cyproheptadine Hydrochloride | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62135-236 | CYPROHEPTADINE HYDROCHLORIDE TABLET [CHARTWELL RX, LLC] | 2 | Current NDC, 1 package rows | 20230129_029ed3b6-175e-4a1a-81ed-350bff5f6167.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 62135-236-90 | 62135023690 | 90 TABLET in 1 BOTTLE (62135-236-90) | 90 tablet | 2023-01-05 | No | No | Historical |