Nadolol
- Product NDC
- 59762-0810
- 11-digit product format
- 597620810
- Labeler code
- 59762
- Product ID
- 59762-0810_7414b083-abf1-44ea-a454-3d58bcfd6139
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- nadolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Greenstone LLC
- Application
- NDA018063
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2014-04-28
- Marketing end
- 0000-00-00
- Substance
- NADOLOL
- Active strength
- 20 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 59762-0810-1 | 59762081001 | 100 TABLET in 1 BOTTLE (59762-0810-1) | 100 tablet | 2014-04-28 | 0000-00-00 | No | No | Current |