NDC 71205-898 – Albuterol
Albuterol Sulfate 2 mg/1 · Tablet · Oral
Product NDC71205-898
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 2 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 71205-898-00 | 100 TABLET in 1 BOTTLE (71205-898-00) | Jul 30, 2021 |
| 71205-898-11 | 1000 TABLET in 1 BOTTLE (71205-898-11) | Jul 30, 2021 |
| 71205-898-30 | 30 TABLET in 1 BOTTLE (71205-898-30) | Jul 30, 2021 |
| 71205-898-55 | 500 TABLET in 1 BOTTLE (71205-898-55) | Jul 30, 2021 |
| 71205-898-60 | 60 TABLET in 1 BOTTLE (71205-898-60) | Jul 30, 2021 |
| 71205-898-90 | 90 TABLET in 1 BOTTLE (71205-898-90) | Jul 30, 2021 |
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