atenolol
- Product NDC
- 72189-152
- 11-digit product format
- 721890152
- Labeler code
- 72189
- Product ID
- 72189-152_4c5d3e5c-d1d9-1368-e063-6294a90ac701
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- direct rx
- Application
- ANDA077443
- Marketing category
- ANDA
- Marketing start
- 2020-11-10
- Substance
- ATENOLOL
- Active strength
- 100 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- atenolol
- Listing expiration
- 2027-12-31
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 |
|---|
| 72189-152-30 | atenolol | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
| 72189-152-90 | atenolol | 90 in 1 BOTTLE | TABLET | 90 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-152 | ATENOLOL TABLET [DIRECT RX] | 2 | Current NDC, Legacy NDC, 2 package rows | 20250119_b3c757de-1cbf-61f5-e053-2995a90accfc.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 |
|---|
| 72189-152-30 | 72189015230 | 30 TABLET in 1 BOTTLE (72189-152-30) | 30 tablet | 2020-11-10 | | No | No | Current |
| 72189-152-90 | 72189015290 | 90 TABLET in 1 BOTTLE (72189-152-90) | 90 tablet | 2020-11-10 | 0000-00-00 | No | No | Current |