Atenolol
- Product NDC
- 68071-3851
- 11-digit product format
- 680713851
- Labeler code
- 68071
- Product ID
- 68071-3851_426703da-1cb8-fb58-e063-6394a90abdec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA078512
- Marketing category
- ANDA
- Marketing start
- 2007-10-31
- Substance
- ATENOLOL
- Active strength
- 100 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 | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 50VV3VW0TI |
| Rxcui | 197379 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-3851-3 | Atenolol | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
| 68071-3851-6 | Atenolol | 60 in 1 BOTTLE | TABLET | 60 | | 3 |
| 68071-3851-9 | Atenolol | 90 in 1 BOTTLE | TABLET | 90 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-3851-3 | 68071385103 | 30 TABLET in 1 BOTTLE (68071-3851-3) | 30 tablet | 2025-10-13 | No | No | Historical |
| 68071-3851-6 | 68071385106 | 60 TABLET in 1 BOTTLE (68071-3851-6) | 60 tablet | 2025-10-30 | No | No | Historical |
| 68071-3851-9 | 68071385109 | 90 TABLET in 1 BOTTLE (68071-3851-9) | 90 tablet | 2025-09-29 | No | No | Historical |