Cyproheptadine Hydrochloride 70710-1110
Product NDC
70710-1110- Manufacturer
- Zydus Pharmaceuticals Usa Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 20, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA208938
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Cyproheptadine Hydrochloride | 4 mg/1 |
Packaging Options(2)
1000 TABLET in 1 BOTTLE (70710-1110-0)
100 TABLET in 1 BOTTLE (70710-1110-1)