NDC 50742-190 – Cyproheptadine Hydrochloride
Cyproheptadine Hydrochloride 4 mg/1 · Tablet · Oral
Product NDC50742-190
Product details
- Brand name
- Cyproheptadine Hydrochloride
- Generic name
- Cyproheptadine Hydrochloride
- Labeler
- Ingenus Pharmaceuticals LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA205087
- Marketed since
- September 23, 2015
- 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 |
|---|---|---|
| 50742-190-01 | 100 TABLET in 1 BOTTLE, PLASTIC (50742-190-01) | Sep 23, 2015 |
| 50742-190-10 | 1000 TABLET in 1 BOTTLE, PLASTIC (50742-190-10) | Sep 23, 2015 |
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