Atenolol
- Product NDC
- 50090-2760
- 11-digit product format
- 500902760
- Labeler code
- 50090
- Product ID
- 50090-2760_3fe49327-8511-467d-9061-13d475dd97e4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA073026
- Marketing category
- ANDA
- Marketing start
- 1991-09-17
- Marketing end
- 0000-00-00
- Substance
- ATENOLOL
- Active strength
- 100 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#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-2760-5 | Atenolol | 90 in 1 BOTTLE | TABLET | 90 | | 11 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2760 | ATENOLOL TABLET [A-S MEDICATION SOLUTIONS] | 11 | Legacy NDC, 1 package rows | 20200122_e6611d33-f4c7-40c4-8db8-6f43c85d444c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-2760-5 | 50090276005 | 90 in 1 BOTTLE | Historical |