Labetalol HCl
- Product NDC
- 68001-205
- 11-digit product format
- 680010205
- Labeler code
- 68001
- Product ID
- 68001-205_9906473a-c9c4-46bf-e053-2995a90abc7e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Labetalol HCl
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- BluePoint Laboratories
- Application
- ANDA075113
- Marketing category
- ANDA
- Marketing start
- 2014-02-26
- Marketing end
- 2021-07-31
- 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 |
|---|
| 68001-205-00 | 68001020500 | 100 TABLET, FILM COATED in 1 BOTTLE (68001-205-00) | 2014-02-26 | 2021-07-31 | No | No | Current |
| 68001-205-03 | 68001020503 | 500 TABLET, FILM COATED in 1 BOTTLE (68001-205-03) | 2014-02-26 | 2021-07-31 | No | No | Current |