Drug application
ALBUTEROL SULFATE (ALBUTEROL SULFATE)
Drugs@FDA ANDA 072637 · SUN PHARM INDUSTRIES
Key facts
| Drug name | ALBUTEROL SULFATE |
|---|---|
| Active ingredients | ALBUTEROL SULFATE |
| Application type | ANDA |
| Application number | 072637 |
| Company | SUN PHARM INDUSTRIES |
| Dosage forms | TABLET, ORAL |
| Strength | EQ 4MG BASE |
| Marketing status | Prescription |
| TE codes | AB |
| Reference listed drug | No |
| Latest submission status date | Feb 1, 1989 |
At a glance
- 1–9 Submissions
- 10–99 Supplements
- None Label versions
- 1–9 Products
- 1–9 Therapeutic equivalents
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Drugs@FDA applications
Drugs@FDA covers FDA-approved brand-name and generic drugs and therapeutic biologics, with their applications (NDA, ANDA or BLA), products, submissions and labels.