Carvedilol
- Product NDC
- 0093-7296
- 11-digit product format
- 000937296
- Labeler code
- 0093
- Product ID
- 0093-7296_3d07d8c6-ffea-41c3-a50c-4e3d723de14f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carvedilol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA076373
- Marketing category
- ANDA
- Marketing start
- 2007-09-06
- Substance
- CARVEDILOL
- Active strength
- 25 mg/1
- Pharmacologic classes
- Adrenergic alpha-Antagonists [MoA], Adrenergic beta1-Antagonists [MoA], Adrenergic beta2-Antagonists [MoA], alpha-Adrenergic Blocker [EPC], 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
- Carvedilol
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CARVEDILOL | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0K47UL67F2 |
| Rxcui | 200031, 200032, 200033, 686924 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0093-7296-01 | Carvedilol | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 16 |
| 0093-7296-05 | Carvedilol | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | | 16 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| CARVEDILOL | ACTIVE INGREDIENT | 0K47UL67F2 | CARVEDILOL TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 10 | |
| CARVEDILOL | ACTIVE MOIETY | 0K47UL67F2 | CARVEDILOL TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 10 | |
| CROSPOVIDONE | INACTIVE INGREDIENT | 68401960MK | CARVEDILOL TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 10 | |
| HYPROMELLOSE 2910 (3 MPA.S) | INACTIVE INGREDIENT | 0VUT3PMY82 | CARVEDILOL TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 10 | |
| HYPROMELLOSE 2910 (5 MPA.S) | INACTIVE INGREDIENT | R75537T0T4 | CARVEDILOL TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 10 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | CARVEDILOL TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 10 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | CARVEDILOL TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 10 | |
| POLYETHYLENE GLYCOL 400 | INACTIVE INGREDIENT | B697894SGQ | CARVEDILOL TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 10 | |
| POLYSORBATE 80 | INACTIVE INGREDIENT | 6OZP39ZG8H | CARVEDILOL TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 10 | |
| POVIDONE K30 | INACTIVE INGREDIENT | U725QWY32X | CARVEDILOL TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 10 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | CARVEDILOL TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 10 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | CARVEDILOL TABLET, FILM COATED [TEVA PHARMACEUTICALS USA INC] | 10 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0093-7296 | CARVEDILOL TABLET, FILM COATED [TEVA PHARMACEUTICALS USA, INC.] | 16 | Current NDC, Legacy NDC, 2 package rows | 20240426_68c275e8-992a-4520-8065-ab6d615d89cc.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0093-7296-01 | 00093729601 | 100 TABLET, FILM COATED in 1 BOTTLE (0093-7296-01) | 2007-09-06 | 0000-00-00 | No | No | Current |
| 0093-7296-05 | 00093729605 | 500 TABLET, FILM COATED in 1 BOTTLE (0093-7296-05) | 2008-12-02 | 0000-00-00 | No | No | Current |