Labetalol HCl
- Product NDC
- 60760-610
- 11-digit product format
- 607600610
- Labeler code
- 60760
- Product ID
- 60760-610_85cd688a-25c6-194d-e053-2991aa0aa5d0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Labetalol HCl
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA075113
- Marketing category
- ANDA
- Marketing start
- 2019-04-05
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-610-90 | 60760061090 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-610-90) | 2019-04-05 | 0000-00-00 | No | No | Current |