Atenolol
- Product NDC
- 64205-078
- 11-digit product format
- 642050078
- Labeler code
- 64205
- Product ID
- 64205-078_0217e704-e3f3-4c71-aa01-106adb9ff9c8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ReadyMeds
- Application
- ANDA074052
- Marketing category
- ANDA
- Marketing start
- 1992-05-01
- Marketing end
- 0000-00-00
- Substance
- ATENOLOL
- Active strength
- 25 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 64205-078-30 | Atenolol | 30 in 1 BOTTLE | TABLET | 30 | | 15 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64205-078 | ATENOLOL TABLET [READYMEDS] | 15 | Legacy NDC, 1 package rows | 20140702_bfe631e8-ab7d-40d0-b42e-ed1102955c44.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 64205-078-30 | 64205007830 | 30 in 1 BOTTLE | Historical |