Atenolol
- Product NDC
- 50090-2811
- 11-digit product format
- 500902811
- Labeler code
- 50090
- Product ID
- 50090-2811_1c530b16-6e36-4f78-9040-a3720813df50
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA073457
- Marketing category
- ANDA
- Marketing start
- 1992-01-24
- 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
- 2019-12-31
- 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 |
|---|
| 50090-2811-0 | Atenolol | 1 in 1 BLISTER PACK | TABLET | 1 | | 6 |
| 50090-2811-0 | Atenolol | 32 in 1 BOX, UNIT-DOSE | TABLET | 32 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2811 | ATENOLOL TABLET [A-S MEDICATION SOLUTIONS] | 6 | Legacy NDC, 2 package rows | 20190225_1eed54d1-2ec4-44a6-b0e5-6dc3a66dba19.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-2811-0 | 50090281100 | 1 in 1 BLISTER PACK | Historical |