Atenolol
- Product NDC
- 83008-052
- 11-digit product format
- 830080052
- Labeler code
- 83008
- Product ID
- 83008-052_83281585-08d8-4021-90e5-8f5d47422cf4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA213136
- Marketing category
- ANDA
- Marketing start
- 2024-01-25
- Marketing end
- 2027-03-31
- Substance
- ATENOLOL
- Active strength
- 50 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Current FDA listing
- Yes
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 |
|---|
| 83008-052-30 | 83008005230 | 30 TABLET in 1 BOTTLE (83008-052-30) | 30 tablet | 2024-01-25 | 2027-03-31 | No | No | Historical |