Atenolol
- Product NDC
- 68071-3830
- 11-digit product format
- 680713830
- Labeler code
- 68071
- Product ID
- 68071-3830_42ca57a4-29af-ef76-e063-6394a90aa683
- 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
- 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 |
|---|
| 68071-3830-1 | Atenolol | 120 in 1 BOTTLE | TABLET | 120 | | 2 |
| 68071-3830-9 | Atenolol | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-3830 | ATENOLOL TABLET [NUCARE PHARMACEUTICALS,INC.] | 1 | Current NDC, 2 package rows | 20250419_331128cc-f56e-4329-e063-6394a90a5ead.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 |
|---|
| 68071-3830-1 | 68071383001 | 120 TABLET in 1 BOTTLE (68071-3830-1) | 120 tablet | 2025-04-18 | No | No | Current |
| 68071-3830-9 | 68071383009 | 90 TABLET in 1 BOTTLE (68071-3830-9) | 90 tablet | 2025-11-04 | No | No | Current |