FdaApplication
ANDA 070917
Identifiers
- fda_app_no: ANDA070917
Properties
| Property | Value |
|---|---|
| applicant_name | ABBOTT LABORATORIES HOSP PRODUCTS DIV |
| application_type | ANDA |
| approval_date | 1989-02-03 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NALBUPHINE HYDROCHLORIDE | NALBUPHINE HYDROCHLORIDE | 20MG/ML (20MG/ML) | SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS |
1 product