NDC 53489-176 – albuterol sulfate
Albuterol Sulfate 2 mg/1 · Tablet · Oral
Product NDC53489-176
Product details
- Brand name
- albuterol sulfate
- Generic name
- albuterol sulfate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA072637
- Marketed since
- December 5, 1989
- Listing expires
- December 31, 2027
- Pharmacologic class
- beta2-Adrenergic Agonist
Active ingredients
- Albuterol Sulfate 2 mg/1
Uses, dosage, side effects and warnings for Albuterol Sulfate →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 53489-176-01 | 100 TABLET in 1 BOTTLE (53489-176-01) | Dec 5, 1989 |
| 53489-176-02 | 50 TABLET in 1 BOTTLE (53489-176-02) | Dec 5, 1989 |
| 53489-176-03 | 250 TABLET in 1 BOTTLE (53489-176-03) | Dec 5, 1989 |
| 53489-176-05 | 500 TABLET in 1 BOTTLE (53489-176-05) | Dec 5, 1989 |
| 53489-176-10 | 1000 TABLET in 1 BOTTLE (53489-176-10) | Dec 5, 1989 |
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