ATENOLOL
- Product NDC
- 61919-935
- 11-digit product format
- 619190935
- Labeler code
- 61919
- Product ID
- 61919-935_9c5970fb-9b7d-6e87-e053-2a95a90a6889
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ATENOLOL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA076900
- Marketing category
- ANDA
- Marketing start
- 2019-07-29
- 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
- 2021-12-31
- 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 |
|---|
| 61919-935-30 | ATENOLOL | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
| 61919-935-60 | ATENOLOL | 60 in 1 BOTTLE | TABLET | 60 | | 2 |
| 61919-935-90 | 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 |
|---|
| 61919-935 | ATENOLOL TABLET [DIRECT RX] | 2 | Legacy NDC, 2 package rows | 20170719_494b88fa-a2b7-4835-e054-00144ff8d46c.zip |
| 61919-935 | ATENOLOL TABLET [DIRECT_RX] | 2 | Legacy NDC, 1 package rows | 20200118_8ed726e8-8174-55f8-e053-2a95a90a8716.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 |
|---|
| 61919-935-30 | 61919093530 | 30 in 1 BOTTLE | | | | | | Historical |
| 61919-935-60 | 61919093560 | 60 in 1 BOTTLE | | | | | | Historical |
| 61919-935-90 | 61919093590 | 90 TABLET in 1 BOTTLE (61919-935-90) | 90 tablet | 2019-07-29 | 0000-00-00 | No | No | Current |