Labetalol HCl
- Product NDC
- 70518-0534
- 11-digit product format
- 705180534
- Labeler code
- 70518
- Product ID
- 70518-0534_85a8272b-8756-c511-e053-2a91aa0a4509
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Labetalol HCl
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075113
- Marketing category
- ANDA
- Marketing start
- 2017-05-15
- 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