NDC 59762-3721 – Alprazolam
Alprazolam 1 mg/1 · Tablet · Oral
Product NDC59762-3721
Product details
- Brand name
- Alprazolam
- Generic name
- alprazolam
- Labeler
- Mylan Pharmaceuticals Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- NDA AUTHORIZED GENERIC · NDA018276
- Marketed since
- October 16, 1981
- Listing expires
- December 31, 2026
- Pharmacologic class
- Benzodiazepine
Active ingredients
- Alprazolam 1 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 59762-3721-1 | 100 TABLET in 1 BOTTLE (59762-3721-1) | Oct 16, 1981 |
| 59762-3721-3 | 500 TABLET in 1 BOTTLE (59762-3721-3) | Oct 16, 1981 |
| 59762-3721-4 | 1000 TABLET in 1 BOTTLE (59762-3721-4) | Oct 16, 1981 |
Recalls mentioning this NDC
- D-0326-2015 Dec 31, 2014 · Class II
Subpotent Drug
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