Atenolol
- Product NDC
- 33261-349
- 11-digit product format
- 332610349
- Labeler code
- 33261
- Product ID
- 33261-349_e821edd9-cd2c-4f50-92a2-ab13a5823e86
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aidarex Pharmaceuticals LLC
- Application
- ANDA077877
- Marketing category
- ANDA
- Marketing start
- 2007-12-04
- 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#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| faf41ef3-b4b3-a29e-3b26-07c3009003bf | Product name | 5 | 20220517 |
| 5eb1a708-d713-e905-0a08-b103c64796f4 | Product name | 3 | 20201019 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 33261-349-10 | 2020-01-31 | C162847 | 48780-1 | 9d75b9cf-d7ff-f424-e053-dadaa90a57ce | Atenolol Tablets, USP |
| 33261-349-30 | 2020-01-31 | C162847 | 48780-1 | 9d75b9cf-d7ff-f424-e053-dadaa90a57ce | Atenolol Tablets, USP |
| 33261-349-60 | 2020-01-31 | C162847 | 48780-1 | 9d75b9cf-d7ff-f424-e053-dadaa90a57ce | Atenolol Tablets, USP |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 33261-349-10 | Atenolol | 1000 in 1 BOTTLE | TABLET | 1000 | 3 | |
| 33261-349-30 | Atenolol | 30 in 1 BOTTLE | TABLET | 30 | 3 | |
| 33261-349-60 | Atenolol | 60 in 1 BOTTLE | TABLET | 60 | 3 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 33261-349-30 | EA - Each | 33261-349 | 7706e47d-e9b1-42ea-baa0-0de825d8f955 | 1 | 2015-10-02 |
| 33261-349-60 | EA - Each | 33261-349 | 1f854366-0685-47c1-a4f7-a4f0b9c34ada | 1 | 2015-10-02 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| ATENOLOL | ACTIVE INGREDIENT | 50VV3VW0TI | ATENOLOL TABLET [AIDAREX PHARMACEUTICALS LLC] | 3 | |
| ATENOLOL | ACTIVE MOIETY | 50VV3VW0TI | ATENOLOL TABLET [AIDAREX PHARMACEUTICALS LLC] | 3 | |
| MAGNESIUM CARBONATE | INACTIVE INGREDIENT | 0E53J927NA | ATENOLOL TABLET [AIDAREX PHARMACEUTICALS LLC] | 3 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | ATENOLOL TABLET [AIDAREX PHARMACEUTICALS LLC] | 3 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | ATENOLOL TABLET [AIDAREX PHARMACEUTICALS LLC] | 3 | |
| SODIUM LAURYL SULFATE | INACTIVE INGREDIENT | 368GB5141J | ATENOLOL TABLET [AIDAREX PHARMACEUTICALS LLC] | 3 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | ATENOLOL TABLET [AIDAREX PHARMACEUTICALS LLC] | 3 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | ATENOLOL TABLET [AIDAREX PHARMACEUTICALS LLC] | 3 |
DailyMed Dashboard NDC Coverage#
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 197379 | atenolol 100 MG Oral Tablet | PSN | 3ee0fa02-8fcc-4b56-98a7-1f636ae0bd74 | 3 |
| 197380 | atenolol 25 MG Oral Tablet | PSN | 3ee0fa02-8fcc-4b56-98a7-1f636ae0bd74 | 3 |
| 197381 | atenolol 50 MG Oral Tablet | PSN | 3ee0fa02-8fcc-4b56-98a7-1f636ae0bd74 | 3 |
| 197379 | atenolol 100 MG Oral Tablet | SCD | 3ee0fa02-8fcc-4b56-98a7-1f636ae0bd74 | 3 |
| 197380 | atenolol 25 MG Oral Tablet | SCD | 3ee0fa02-8fcc-4b56-98a7-1f636ae0bd74 | 3 |
| 197381 | atenolol 50 MG Oral Tablet | SCD | 3ee0fa02-8fcc-4b56-98a7-1f636ae0bd74 | 3 |
Packages#
| Package NDC | 11-digit format | Description | Status |
|---|---|---|---|
| 33261-349-10 | 33261034910 | 1000 in 1 BOTTLE | Historical |
| 33261-349-30 | 33261034930 | 30 in 1 BOTTLE | Historical |
| 33261-349-60 | 33261034960 | 60 in 1 BOTTLE | Historical |