Labetalol Hydrochloride
- Product NDC
- 60760-231
- 11-digit product format
- 607600231
- Labeler code
- 60760
- Product ID
- 60760-231_7abab1f2-c4c6-0b9b-e053-2a91aa0abad4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- labetalol hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- NDA018716
- Marketing category
- NDA
- Marketing start
- 2014-12-01
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-231-90 | 60760023190 | 90 TABLET in 1 BOTTLE, PLASTIC (60760-231-90) | 90 tablet | 2017-11-21 | 0000-00-00 | No | No | Current |