Labetalol hydrochloride
- Product NDC
- 63629-5268
- 11-digit product format
- 636295268
- Labeler code
- 63629
- Product ID
- 63629-5268_59212119-691b-49de-aa65-a2a10a1035ba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Labetalol hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075133
- Marketing category
- ANDA
- Marketing start
- 1998-08-03
- Marketing end
- 0000-00-00
- Substance
- LABETALOL HYDROCHLORIDE
- Active strength
- 200 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-5268-1 | 63629526801 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-5268-1) | 2014-03-25 | 0000-00-00 | No | No | Current |
| 63629-5268-2 | 63629526802 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-5268-2) | 2014-03-25 | 0000-00-00 | No | No | Current |
| 63629-5268-3 | 63629526803 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-5268-3) | 2014-03-25 | 0000-00-00 | No | No | Current |