Nadolol
- Product NDC
- 51407-979
- 11-digit product format
- 514070979
- Labeler code
- 51407
- Product ID
- 51407-979_4b31bd46-93da-ed99-e063-6394a90a827f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nadolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA210955
- Marketing category
- ANDA
- Marketing start
- 2018-07-23
- Substance
- NADOLOL
- Active strength
- 80 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| FEN504330V | NADOLOL | 42200-33-9 | NADOLOL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51407-979-01 | 51407097901 | 100 TABLET in 1 BOTTLE (51407-979-01) | 100 tablet | 2025-04-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Nadolol Tablets, USP | Golden State Medical Supply, Inc. | 2026-02-19 | HUMAN PRESCRIPTION DRUG LABEL | 2 |