NDC 64980-504 – Cyproheptadine Hydrochloride
Cyproheptadine Hydrochloride 2 mg/5mL · Syrup · Oral
Product NDC64980-504
Product details
- Brand name
- Cyproheptadine Hydrochloride
- Generic name
- Cyproheptadine Hydrochloride
- Labeler
- Rising Pharma Holdings, Inc.
- Dosage form
- Syrup
- Route
- Oral
- Marketing category
- ANDA · ANDA040668
- Marketed since
- July 10, 2006
- Listing expires
- December 31, 2026
Active ingredients
- Cyproheptadine Hydrochloride 2 mg/5mL
Uses, dosage, side effects and warnings for Cyproheptadine Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 64980-504-48 | 473 mL in 1 BOTTLE (64980-504-48) | Jul 10, 2006 |
Recalls mentioning this NDC
- D-0724-2026 Jul 29, 2026 · Class II
Presence of Precipitate: medication was crystallizing and particles floating in the bottle
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