CYPROHEPTADINE HYDROCHLORIDE
- Product NDC
- 42708-187
- 11-digit product format
- 427080187
- Labeler code
- 42708
- Product ID
- 42708-187_45870b44-8f41-56a7-e063-6394a90a6ecf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CYPROHEPTADINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- QPharma Inc
- 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 |
|---|
| 42708-187-21 | CYPROHEPTADINE HYDROCHLORIDE | 21 in 1 BOTTLE, PLASTIC | TABLET | 21 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42708-187 | CYPROHEPTADINE HYDROCHLORIDE TABLET [QPHARMA INC] | 1 | Current NDC, 1 package rows | 20240727_1dfe4478-76d9-9b8f-e063-6394a90aefe8.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 |
|---|
| 42708-187-21 | 42708018721 | 21 TABLET in 1 BOTTLE, PLASTIC (42708-187-21) | 21 tablet | 2024-07-26 | Yes | No | Current |