FdaApplication
ANDA 070918
Identifiers
- fda_app_no: ANDA070918
Properties
| Property | Value |
|---|---|
| applicant_name | HOSPIRA INC |
| application_type | ANDA |
| approval_date | 1989-02-03 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NALBUPHINE HYDROCHLORIDE | NALBUPHINE HYDROCHLORIDE | 200MG/10ML (20MG/ML) | SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS |
1 product