Bisoprolol
- Product NDC
- 72162-2177
- 11-digit product format
- 721622177
- Labeler code
- 72162
- Product ID
- 72162-2177_134a42de-4b00-48ab-bd5e-8061b1ee3ff5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bisoprolol fumarate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075474
- Marketing category
- ANDA
- Marketing start
- 2019-06-20
- Substance
- BISOPROLOL FUMARATE
- Active strength
- 5 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
- Bisoprolol
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BISOPROLOL FUMARATE | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | UR59KN573L |
| Rxcui | 854905 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2177-1 | Bisoprolol | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 100 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2177 | BISOPROLOL (BISOPROLOL FUMARATE) TABLET, FILM COATED [BRYANT RANCH PREPACK] | 100 | Current NDC, 1 package rows | 20231212_78056d0b-2265-4da3-a4fe-b96d98289848.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2177-1 | 72162217701 | 100 TABLET, FILM COATED in 1 BOTTLE (72162-2177-1) | 2023-12-07 | No | No | Current |