Atenolol
- Product NDC
- 21695-324
- 11-digit product format
- 216950324
- Labeler code
- 21695
- Product ID
- 21695-324_d3e90e8f-d3c9-4c73-975f-206a28e0b103
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rebel Distributors Corp.
- Application
- ANDA073352
- Marketing category
- ANDA
- Marketing start
- 1991-12-27
- 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
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|---|---|---|---|---|
| 21695-324-30 | 2019-09-24 | C162847 | 48780-1 | 934fe258-4d01-48b1-e053-8cdaa90a720a | Atenolol Tablets, USP |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 21695-324-30 | Atenolol | 30 in 1 BOTTLE | TABLET | 30 | 1 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 21695-324-30 | EA - Each | 21695-324 | 2d1760d4-602c-4511-a044-6cc5fddb5a05 | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| ATENOLOL | ACTIVE INGREDIENT | 50VV3VW0TI | ATENOLOL TABLET [REBEL DISTRIBUTORS CORP.] | 1 | |
| ATENOLOL | ACTIVE MOIETY | 50VV3VW0TI | ATENOLOL TABLET [REBEL DISTRIBUTORS CORP.] | 1 | |
| COLLOIDAL SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | ATENOLOL TABLET [REBEL DISTRIBUTORS CORP.] | 1 | |
| MAGNESIUM CARBONATE | INACTIVE INGREDIENT | 0E53J927NA | ATENOLOL TABLET [REBEL DISTRIBUTORS CORP.] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | ATENOLOL TABLET [REBEL DISTRIBUTORS CORP.] | 1 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | ATENOLOL TABLET [REBEL DISTRIBUTORS CORP.] | 1 | |
| SODIUM LAURYL SULFATE | INACTIVE INGREDIENT | 368GB5141J | ATENOLOL TABLET [REBEL DISTRIBUTORS CORP.] | 1 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | ATENOLOL TABLET [REBEL DISTRIBUTORS CORP.] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | ATENOLOL TABLET [REBEL DISTRIBUTORS CORP.] | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 197379 | atenolol 100 MG Oral Tablet | PSN | aae36822-9c1b-4600-81d6-da022d56c03e | 1 |
| 197381 | atenolol 50 MG Oral Tablet | PSN | aae36822-9c1b-4600-81d6-da022d56c03e | 1 |
| 197379 | atenolol 100 MG Oral Tablet | SCD | aae36822-9c1b-4600-81d6-da022d56c03e | 1 |
| 197381 | atenolol 50 MG Oral Tablet | SCD | aae36822-9c1b-4600-81d6-da022d56c03e | 1 |
Packages#
| Package NDC | 11-digit format | Description | Status |
|---|---|---|---|
| 21695-324-30 | 21695032430 | 30 in 1 BOTTLE | Historical |