Nadolol
- Product NDC
- 72162-2234
- 11-digit product format
- 721622234
- Labeler code
- 72162
- Product ID
- 72162-2234_14d427a2-ac49-4805-95c2-79e3151ea616
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nadolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203455
- Marketing category
- ANDA
- Marketing start
- 2016-02-23
- Substance
- NADOLOL
- Active strength
- 20 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- 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 |
|---|
| 72162-2234-1 | 72162223401 | 100 TABLET in 1 BOTTLE (72162-2234-1) | 100 tablet | 2024-01-26 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Rx Only | Bryant Ranch Prepack | 2024-01-26 | HUMAN PRESCRIPTION DRUG LABEL | 100 |