NDC 0121-0646 – Amantadine Hydrochloride
Amantadine Hydrochloride 50 mg/5mL · Solution · Oral
Product NDC0121-0646
Product details
- Brand name
- Amantadine Hydrochloride
- Generic name
- Amantadine Hydrochloride
- Labeler
- PAI Holdings, LLC dba PAI Pharma
- Dosage form
- Solution
- Route
- Oral
- Marketing category
- ANDA · ANDA074509
- Marketed since
- July 17, 1995
- Listing expires
- December 31, 2026
- Pharmacologic class
- Influenza A M2 Protein Inhibitor
Active ingredients
- Amantadine Hydrochloride 50 mg/5mL
Uses, dosage, side effects and warnings for Amantadine Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0121-0646-10 | 10 TRAY in 1 CASE (0121-0646-10) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE | Jul 17, 1995 |
| 0121-0646-16 | 473 mL in 1 BOTTLE (0121-0646-16) | Jul 17, 1995 |
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