Carvedilol
- Product NDC
- 68001-152
- 11-digit product format
- 680010152
- Labeler code
- 68001
- Product ID
- 68001-152_4c082ad1-65d7-7db1-e063-6394a90a3f8e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carvedilol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- BluePoint Laboratories
- Application
- ANDA077614
- Marketing category
- ANDA
- Marketing start
- 2014-04-22
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Carvedilol
- Listing expiration
- 2027-12-31
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 |
|---|
| 68001-152-00 | Carvedilol | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 14 |
| 68001-152-03 | Carvedilol | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | | 14 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| CARVEDILOL | ACTIVE INGREDIENT | 0K47UL67F2 | CARVEDILOL TABLET, FILM COATED [BLUEPOINT LABORATORIES] | 3 | |
| CARVEDILOL | ACTIVE MOIETY | 0K47UL67F2 | CARVEDILOL TABLET, FILM COATED [BLUEPOINT LABORATORIES] | 3 | |
| CROSPOVIDONE | INACTIVE INGREDIENT | 68401960MK | CARVEDILOL TABLET, FILM COATED [BLUEPOINT LABORATORIES] | 3 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | CARVEDILOL TABLET, FILM COATED [BLUEPOINT LABORATORIES] | 3 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | CARVEDILOL TABLET, FILM COATED [BLUEPOINT LABORATORIES] | 3 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | CARVEDILOL TABLET, FILM COATED [BLUEPOINT LABORATORIES] | 3 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | CARVEDILOL TABLET, FILM COATED [BLUEPOINT LABORATORIES] | 3 | |
| POVIDONES | INACTIVE INGREDIENT | FZ989GH94E | CARVEDILOL TABLET, FILM COATED [BLUEPOINT LABORATORIES] | 3 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | CARVEDILOL TABLET, FILM COATED [BLUEPOINT LABORATORIES] | 3 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | CARVEDILOL TABLET, FILM COATED [BLUEPOINT LABORATORIES] | 3 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | CARVEDILOL TABLET, FILM COATED [BLUEPOINT LABORATORIES] | 3 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68001-152 | CARVEDILOL TABLET, FILM COATED [BLUEPOINT LABORATORIES] | 12 | Current NDC, Legacy NDC, 2 package rows | 20231223_e68c9b18-e7fd-45f7-a8f5-1d815e32680b.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 |
|---|
| 68001-152-00 | 68001015200 | 100 TABLET, FILM COATED in 1 BOTTLE (68001-152-00) | 2014-04-22 | 0000-00-00 | No | No | Current |
| 68001-152-03 | 68001015203 | 500 TABLET, FILM COATED in 1 BOTTLE (68001-152-03) | 2014-04-22 | 0000-00-00 | No | No | Current |