LABETALOL HYDROCHLORIDE
- Product NDC
- 50090-6774
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Labetalol Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA211953
- Marketing category
- ANDA
- Substance
- LABETALOL HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-6774-0 | 100 TABLET, FILM COATED in 1 BOTTLE (50090-6774-0) | 2023-10-24 | | No | Historical |
| 50090-6774-1 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-6774-1) | 2023-10-24 | | No | Historical |