Labetalol hydrochloride
- Product NDC
- 60429-277
- 11-digit product format
- 604290277
- Labeler code
- 60429
- Product ID
- 60429-277_7a07f7b3-78aa-0d61-e053-2a91aa0aa0e3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Labetalol hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA075133
- Marketing category
- ANDA
- Marketing start
- 2013-04-16
- Marketing end
- 0000-00-00
- Substance
- LABETALOL HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record