Labetalol HCl
- Product NDC
- 0185-0010
- 11-digit product format
- 001850010
- Labeler code
- 0185
- Product ID
- 0185-0010_a4c308a8-e7f2-4f2f-b2f5-2cf74022a372
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Labetalol HCl
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Eon Labs, Inc.
- Application
- ANDA075113
- Marketing category
- ANDA
- Marketing start
- 1998-08-04
- Marketing end
- 2023-09-30
- 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
- 0000-00-00
- 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 |
|---|
| 0185-0010-01 | 00185001001 | 100 TABLET, FILM COATED in 1 BOTTLE (0185-0010-01) | 1998-08-04 | 0000-00-00 | No | No | Current |
| 0185-0010-05 | 00185001005 | 500 TABLET, FILM COATED in 1 BOTTLE (0185-0010-05) | 1998-08-04 | 0000-00-00 | No | No | Current |
| 0185-0010-10 | 00185001010 | 1000 TABLET, FILM COATED in 1 BOTTLE (0185-0010-10) | 1998-08-04 | 0000-00-00 | No | No | Current |