Atenolol
- Product NDC
- 72162-2325
- 11-digit product format
- 721622325
- Labeler code
- 72162
- Product ID
- 72162-2325_927127b5-6f5f-48d4-b1f9-fdac0b4669eb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA073026
- Marketing category
- ANDA
- Marketing start
- 2022-12-19
- Substance
- ATENOLOL
- Active strength
- 50 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Atenolol
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ATENOLOL | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 50VV3VW0TI |
| Rxcui | 197381 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2325-0 | Atenolol | 1000 in 1 BOTTLE | TABLET | 1000 | | 100 |
| 72162-2325-9 | Atenolol | 90 in 1 BOTTLE | TABLET | 90 | | 100 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2325 | ATENOLOL TABLET [BRYANT RANCH PREPACK] | 100 | Current NDC, 2 package rows | 20240606_ecfcebcc-8fcd-48e6-871e-151074df3abc.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2325-0 | 72162232500 | 1000 TABLET in 1 BOTTLE (72162-2325-0) | 1000 tablet | 2024-06-05 | No | No | Historical |
| 72162-2325-9 | 72162232509 | 90 TABLET in 1 BOTTLE (72162-2325-9) | 90 tablet | 2024-06-05 | No | No | Historical |