NDC 71205-899 – Albuterol
Albuterol Sulfate 4 mg/1 · Tablet · Oral
Product NDC71205-899
Product details
- Brand name
- Albuterol
- Generic name
- Albuterol
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA207046
- Marketed since
- June 29, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- beta2-Adrenergic Agonist
Active ingredients
- Albuterol Sulfate 4 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 71205-899-00 | 100 TABLET in 1 BOTTLE (71205-899-00) | Jul 30, 2021 |
| 71205-899-11 | 1000 TABLET in 1 BOTTLE (71205-899-11) | Jul 30, 2021 |
| 71205-899-30 | 30 TABLET in 1 BOTTLE (71205-899-30) | Jul 30, 2021 |
| 71205-899-55 | 500 TABLET in 1 BOTTLE (71205-899-55) | Jul 30, 2021 |
| 71205-899-60 | 60 TABLET in 1 BOTTLE (71205-899-60) | Jul 30, 2021 |
| 71205-899-90 | 90 TABLET in 1 BOTTLE (71205-899-90) | Jul 30, 2021 |
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- 63629-2611 Albuterol Sulfate 4 mg/1 · Tablet · Bryant Ranch Prepack
- 71205-898 Albuterol Sulfate 2 mg/1 · Tablet · Proficient Rx LP
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- 70771-1512 Albuterol Sulfate 4 mg/1 · Tablet · Zydus Lifesciences Limited
- 70710-1061 Albuterol Sulfate 2 mg/1 · Tablet · Zydus Pharmaceuticals USA Inc.
- 70710-1062 Albuterol Sulfate 4 mg/1 · Tablet · Zydus Pharmaceuticals USA Inc.