ATENOLOL
- Product NDC
- 72189-135
- 11-digit product format
- 721890135
- Labeler code
- 72189
- Product ID
- 72189-135_2bed0337-ef1e-1146-e063-6394a90a48fd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ATENOLOL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- direct rx
- Application
- ANDA077443
- Marketing category
- ANDA
- Marketing start
- 2020-12-02
- 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 | 197380, 197381 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-135-30 | ATENOLOL | 30 in 1 BOTTLE | TABLET | 30 | | 9 |
| 72189-135-90 | ATENOLOL | 90 in 1 BOTTLE | TABLET | 90 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-135 | ATENOLOL TABLET ATENOLOL TABLET [DIRECT RX] | 9 | Current NDC, Legacy NDC, 2 package rows | 20250119_b3d9f826-7ed7-1e3b-e053-2995a90ae731.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 |
|---|
| 72189-135-30 | 72189013530 | 30 TABLET in 1 BOTTLE (72189-135-30) | 30 tablet | 2020-12-02 | 0000-00-00 | No | No | Current |
| 72189-135-90 | 72189013590 | 90 TABLET in 1 BOTTLE (72189-135-90) | 90 tablet | 2020-12-02 | 0000-00-00 | No | No | Current |