Cyproheptadine Hydrochloride 42708-0187
Product NDC
42708-0187- Manufacturer
- Qpharma Inc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 24, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA212491
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Cyproheptadine Hydrochloride | 4 mg/1 |
Packaging Options(1)
21 TABLET in 1 BOTTLE, PLASTIC (42708-187-21)