Atenolol
- Product NDC
- 70934-458
- 11-digit product format
- 709340458
- Labeler code
- 70934
- Product ID
- 70934-458_b7ae9583-b5b1-97e3-e053-2a95a90a701d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA073026
- Marketing category
- ANDA
- Marketing start
- 2019-10-30
- Marketing end
- 0000-00-00
- Substance
- ATENOLOL
- Active strength
- 100 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 50VV3VW0TI | ATENOLOL | 29122-68-7 | ATENOLOL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-458-30 | 70934045830 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-458-30) | 30 tablet | 2019-10-30 | 0000-00-00 | No | No | Current |