NDC 52817-415 – Cyproheptadine Hydrochloride
Cyproheptadine Hydrochloride 4 mg/1 · Tablet · Oral
Product NDC52817-415
Product details
- Brand name
- Cyproheptadine Hydrochloride
- Generic name
- Cyproheptadine Hydrochloride
- Labeler
- TRUPHARMA, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA206553
- Marketed since
- June 1, 2026
- Listing expires
- December 31, 2027
Active ingredients
- Cyproheptadine Hydrochloride 4 mg/1
Uses, dosage, side effects and warnings for Cyproheptadine Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 52817-415-10 | 100 TABLET in 1 BOTTLE, PLASTIC (52817-415-10) | Jun 1, 2026 |
| 52817-415-50 | 500 TABLET in 1 BOTTLE, PLASTIC (52817-415-50) | Jun 1, 2026 |
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