Cyproheptadine Hydrochloride 72789-0102
Product NDC
72789-0102- Manufacturer
- Pd-Rx Pharmaceuticals, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 1, 2020
- Listing Expires
- December 31, 2027
- Application
- ANDA206676
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Cyproheptadine Hydrochloride | 4 mg/1 |
Packaging Options(2)
100 TABLET in 1 BOTTLE, PLASTIC (72789-102-01)
30 TABLET in 1 BOTTLE, PLASTIC (72789-102-30)