NDC 71335-0849 – Alprazolam
Alprazolam .5 mg/1 · Tablet · Oral
Product NDC71335-0849
Product details
- Brand name
- Alprazolam
- Generic name
- Alprazolam
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA074342
- Marketed since
- October 1, 1993
- Listing expires
- December 31, 2026
- Pharmacologic class
- Benzodiazepine
Active ingredients
- Alprazolam .5 mg/1
Package NDC codes (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0849-0 | 10 TABLET in 1 BOTTLE (71335-0849-0) | May 2, 2022 |
| 71335-0849-1 | 15 TABLET in 1 BOTTLE (71335-0849-1) | Jun 20, 2018 |
| 71335-0849-2 | 30 TABLET in 1 BOTTLE (71335-0849-2) | Jun 8, 2018 |
| 71335-0849-3 | 20 TABLET in 1 BOTTLE (71335-0849-3) | May 2, 2022 |
| 71335-0849-4 | 100 TABLET in 1 BOTTLE (71335-0849-4) | May 2, 2022 |
| 71335-0849-5 | 90 TABLET in 1 BOTTLE (71335-0849-5) | Sep 6, 2018 |
| 71335-0849-6 | 60 TABLET in 1 BOTTLE (71335-0849-6) | Jun 8, 2018 |
| 71335-0849-7 | 120 TABLET in 1 BOTTLE (71335-0849-7) | May 2, 2022 |
| 71335-0849-8 | 28 TABLET in 1 BOTTLE (71335-0849-8) | May 2, 2022 |
| 71335-0849-9 | 2 TABLET in 1 BOTTLE (71335-0849-9) | Jun 22, 2018 |
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