NDC 0832-0111 – Amantadine Hydrochloride
Amantadine Hydrochloride 100 mg/1 · Tablet · Oral
Product NDC0832-0111
Product details
- Brand name
- Amantadine Hydrochloride
- Generic name
- Amantadine hydrochloride
- Labeler
- Upsher-Smith Laboratories, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076186
- Marketed since
- December 15, 2011
- Marketing end
- February 29, 2028
- Pharmacologic class
- Influenza A M2 Protein Inhibitor
Active ingredients
- Amantadine Hydrochloride 100 mg/1
Uses, dosage, side effects and warnings for Amantadine Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0832-0111-00 | 100 TABLET in 1 BOTTLE (0832-0111-00) | Dec 15, 2011 |
| 0832-0111-50 | 500 TABLET in 1 BOTTLE (0832-0111-50) | Dec 15, 2011 |
Recalls mentioning this NDC
- D-0592-2021 Jun 2, 2021 · Class II
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
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