NDC 71335-0949 – Baclofen
Baclofen 20 mg/1 · Tablet · Oral
Product NDC71335-0949
Product details
- Brand name
- Baclofen
- Generic name
- Baclofen
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA209102
- Marketed since
- April 1, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- gamma-Aminobutyric Acid-ergic Agonist
Active ingredients
- Baclofen 20 mg/1
Package NDC codes (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0949-0 | 120 TABLET in 1 BOTTLE (71335-0949-0) | Oct 31, 2018 |
| 71335-0949-1 | 90 TABLET in 1 BOTTLE (71335-0949-1) | Sep 11, 2018 |
| 71335-0949-2 | 20 TABLET in 1 BOTTLE (71335-0949-2) | May 29, 2024 |
| 71335-0949-3 | 60 TABLET in 1 BOTTLE (71335-0949-3) | Oct 5, 2018 |
| 71335-0949-4 | 45 TABLET in 1 BOTTLE (71335-0949-4) | May 29, 2024 |
| 71335-0949-5 | 112 TABLET in 1 BOTTLE (71335-0949-5) | May 29, 2024 |
| 71335-0949-6 | 30 TABLET in 1 BOTTLE (71335-0949-6) | Sep 6, 2018 |
| 71335-0949-7 | 56 TABLET in 1 BOTTLE (71335-0949-7) | May 29, 2024 |
| 71335-0949-8 | 15 TABLET in 1 BOTTLE (71335-0949-8) | May 29, 2024 |
| 71335-0949-9 | 84 TABLET in 1 BOTTLE (71335-0949-9) | May 29, 2024 |
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