Labetalol Hydrochloride
- Product NDC
- 63629-9300
- 11-digit product format
- 636299300
- Labeler code
- 63629
- Product ID
- 63629-9300_49f28f64-d9a5-40c4-b050-18c265dfc9e7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Labetalol Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075215
- Marketing category
- ANDA
- Marketing start
- 2019-11-22
- Marketing end
- 0000-00-00
- Substance
- LABETALOL
- Active strength
- 200 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 63629-9300-1 | 63629930001 | 500 TABLET, FILM COATED in 1 BOTTLE (63629-9300-1) | 2022-06-06 | 0000-00-00 | No | No | Current |