Labetalol HCl
- Product NDC
- 71335-0733
- 11-digit product format
- 713350733
- Labeler code
- 71335
- Product ID
- 71335-0733_1cc047f3-b3d9-4782-9964-e05b8f1a4339
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Labetalol HCl
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075113
- Marketing category
- ANDA
- Marketing start
- 1998-08-04
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0733-1 | 71335073301 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0733-1) | 1998-08-04 | 0000-00-00 | No | No | Current |
| 71335-0733-2 | 71335073302 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0733-2) | 1998-08-04 | 0000-00-00 | No | No | Current |
| 71335-0733-3 | 71335073303 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0733-3) | 1998-08-04 | 0000-00-00 | No | No | Current |
| 71335-0733-4 | 71335073304 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0733-4) | 1998-08-04 | 0000-00-00 | No | No | Current |