ATENOLOL
- Product NDC
- 61919-854
- 11-digit product format
- 619190854
- Labeler code
- 61919
- Product ID
- 61919-854_ea4edbaa-3901-bf8c-e053-2995a90a0af1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ATENOLOL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA077443
- Marketing category
- ANDA
- Marketing start
- 2019-08-14
- Marketing end
- 0000-00-00
- Substance
- ATENOLOL
- Active strength
- 100 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61919-854-90 | ATENOLOL | 90 in 1 BOTTLE | TABLET | 90 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-854 | ATENOLOL TABLET [DIRECT RX] | 5 | Legacy NDC, 1 package rows | 20190430_b002421f-8120-4e76-a9e2-cc356fbc4cff.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-854-30 | 61919085430 | 30 TABLET in 1 BOTTLE (61919-854-30) | 30 tablet | 2019-08-14 | 0000-00-00 | No | No | Current |
| 61919-854-90 | 61919085490 | 90 TABLET in 1 BOTTLE (61919-854-90) | 90 tablet | 2019-04-29 | 0000-00-00 | No | No | Current |