FdaApplication
ANDA 072072
Identifiers
- fda_app_no: ANDA072072
Properties
| Property | Value |
|---|---|
| applicant_name | IGI LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1989-04-10 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NALBUPHINE HYDROCHLORIDE | NALBUPHINE HYDROCHLORIDE | 10MG/ML (10MG/ML) | SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS |
1 product