NDC 70710-1110 – Cyproheptadine Hydrochloride
Cyproheptadine Hydrochloride 4 mg/1 · Tablet · Oral
Product NDC70710-1110
Product details
- Brand name
- Cyproheptadine Hydrochloride
- Generic name
- Cyproheptadine Hydrochloride
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA208938
- Marketed since
- July 20, 2017
- Listing expires
- December 31, 2026
Active ingredients
- Cyproheptadine Hydrochloride 4 mg/1
Uses, dosage, side effects and warnings for Cyproheptadine Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 70710-1110-0 | 1000 TABLET in 1 BOTTLE (70710-1110-0) | Jul 20, 2017 |
| 70710-1110-1 | 100 TABLET in 1 BOTTLE (70710-1110-1) | Jul 20, 2017 |
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