Atenolol
- Product NDC
- 53808-0660
- 11-digit product format
- 538080660
- Labeler code
- 53808
- Product ID
- 53808-0660_66c085b7-3ec3-43b4-a095-e04cf8d7a76a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- State of Florida DOH Central Pharmacy
- Application
- ANDA078512
- Marketing category
- ANDA
- Marketing start
- 2009-07-01
- 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 |
|---|---|---|---|---|---|
| 53808-0660-1 | 2019-10-21 | C162847 | 48780-1 | 956f9ecf-bfd6-621f-e053-dbdaa90a74ad | Atenolol Tablets, USP |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 53808-0660-1 | Atenolol | 30 in 1 BLISTER PACK | TABLET | 30 | 3 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| ATENOLOL | ACTIVE INGREDIENT | 50VV3VW0TI | ATENOLOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 3 | |
| ATENOLOL | ACTIVE MOIETY | 50VV3VW0TI | ATENOLOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 3 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | ATENOLOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 3 | |
| CROSPOVIDONE | INACTIVE INGREDIENT | 68401960MK | ATENOLOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 3 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | ATENOLOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 3 | |
| POVIDONE K90 | INACTIVE INGREDIENT | RDH86HJV5Z | ATENOLOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 3 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | ATENOLOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 3 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | ATENOLOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 53808-0660 | ATENOLOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 3 | Legacy NDC, 1 package rows | 20100819_97ec87b2-322a-438b-ba95-69040c580eb6.zip |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 197379 | atenolol 100 MG Oral Tablet | PSN | 97ec87b2-322a-438b-ba95-69040c580eb6 | 3 |
| 197380 | atenolol 25 MG Oral Tablet | PSN | 97ec87b2-322a-438b-ba95-69040c580eb6 | 3 |
| 197381 | atenolol 50 MG Oral Tablet | PSN | 97ec87b2-322a-438b-ba95-69040c580eb6 | 3 |
| 197379 | atenolol 100 MG Oral Tablet | SCD | 97ec87b2-322a-438b-ba95-69040c580eb6 | 3 |
| 197380 | atenolol 25 MG Oral Tablet | SCD | 97ec87b2-322a-438b-ba95-69040c580eb6 | 3 |
| 197381 | atenolol 50 MG Oral Tablet | SCD | 97ec87b2-322a-438b-ba95-69040c580eb6 | 3 |
Packages#
| Package NDC | 11-digit format | Description | Status |
|---|---|---|---|
| 53808-0660-1 | 53808066001 | 30 in 1 BLISTER PACK | Historical |