Atenolol 72189-0135
Product NDC
72189-0135- Manufacturer
- Direct Rx
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 2, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA077443
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Atenolol | 50 mg/1 |
Drug Class
beta-Adrenergic Blocker [EPC]Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(2)
30 TABLET in 1 BOTTLE (72189-135-30)
90 TABLET in 1 BOTTLE (72189-135-90)