Cyproheptadine Hydrochloride 52817-0210
Product NDC
52817-0210- Manufacturer
- Trupharma, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 17, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA206553
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Cyproheptadine Hydrochloride | 4 mg/1 |
Packaging Options(2)
100 TABLET in 1 BOTTLE, PLASTIC (52817-210-10)
500 TABLET in 1 BOTTLE, PLASTIC (52817-210-50)