Atenolol
- Product NDC
- 71335-2774
- 11-digit product format
- 713352774
- Labeler code
- 71335
- Product ID
- 71335-2774_12063fb8-2fa7-472a-b32c-ea41f77acbcf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA213136
- Marketing category
- ANDA
- Marketing start
- 2019-11-21
- Substance
- ATENOLOL
- Active strength
- 100 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Atenolol
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ATENOLOL | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 50VV3VW0TI |
| Rxcui | 197379 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2774-1 | 71335277401 | 100 TABLET in 1 BOTTLE (71335-2774-1) | 100 tablet | 2025-10-13 | No | No | Historical |
| 71335-2774-2 | 71335277402 | 30 TABLET in 1 BOTTLE (71335-2774-2) | 30 tablet | 2025-10-13 | No | No | Historical |
| 71335-2774-3 | 71335277403 | 60 TABLET in 1 BOTTLE (71335-2774-3) | 60 tablet | 2025-10-13 | No | No | Historical |
| 71335-2774-4 | 71335277404 | 90 TABLET in 1 BOTTLE (71335-2774-4) | 90 tablet | 2025-10-13 | No | No | Historical |
| 71335-2774-5 | 71335277405 | 20 TABLET in 1 BOTTLE (71335-2774-5) | 20 tablet | 2025-10-13 | No | No | Historical |
| 71335-2774-6 | 71335277406 | 180 TABLET in 1 BOTTLE (71335-2774-6) | 180 tablet | 2025-10-13 | No | No | Historical |
| 71335-2774-7 | 71335277407 | 10 TABLET in 1 BOTTLE (71335-2774-7) | 10 tablet | 2025-10-13 | No | No | Historical |