ATENOLOL
- Product NDC
- 61919-664
- 11-digit product format
- 619190664
- Labeler code
- 61919
- Product ID
- 61919-664_e9d112d7-6f62-05a7-e053-2a95a90a7730
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ATENOLOL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA074056
- Marketing category
- ANDA
- Marketing start
- 2019-10-04
- Marketing end
- 0000-00-00
- Substance
- ATENOLOL
- Active strength
- 50 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 |
|---|
| 61919-664-60 | ATENOLOL | 60 in 1 BOTTLE | TABLET | 60 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-664 | ATENOLOL TABLET [DIRECTRX] | 1 | Legacy NDC, 1 package rows | 20151124_f12b8144-3875-4192-b883-e89e256a89bb.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 |
|---|
| 61919-664-30 | 61919066430 | 50 TABLET in 1 BOTTLE (61919-664-30) | 50 tablet | 2019-10-04 | 0000-00-00 | No | No | Current |
| 61919-664-60 | 61919066460 | 60 in 1 BOTTLE | | | | | | Historical |
| 61919-664-90 | 61919066490 | 90 TABLET in 1 BOTTLE (61919-664-90) | 90 tablet | 2019-10-04 | 0000-00-00 | No | No | Current |