Carvedilol
- Product NDC
- 52959-466
- 11-digit product format
- 529590466
- Labeler code
- 52959
- Product ID
- 52959-466_f145684a-097f-472a-a9fb-ed6c513cdc71
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carvedilol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- H.J. Harkins Company, Inc.
- Application
- ANDA077614
- Marketing category
- ANDA
- Marketing start
- 2007-09-05
- Marketing end
- 0000-00-00
- Substance
- CARVEDILOL
- Active strength
- 6 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 52959-466-30 | Carvedilol | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 1 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| CARVEDILOL | ACTIVE INGREDIENT | 0K47UL67F2 | CARVEDILOL (CARVEDILOL) TABLET, FILM COATED [H.J. HARKINS COMPANY, INC.] | 1 | |
| CARVEDILOL | ACTIVE MOIETY | 0K47UL67F2 | CARVEDILOL (CARVEDILOL) TABLET, FILM COATED [H.J. HARKINS COMPANY, INC.] | 1 | |
| COLLOIDAL SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | CARVEDILOL (CARVEDILOL) TABLET, FILM COATED [H.J. HARKINS COMPANY, INC.] | 1 | |
| CROSPOVIDONE | INACTIVE INGREDIENT | 68401960MK | CARVEDILOL (CARVEDILOL) TABLET, FILM COATED [H.J. HARKINS COMPANY, INC.] | 1 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | CARVEDILOL (CARVEDILOL) TABLET, FILM COATED [H.J. HARKINS COMPANY, INC.] | 1 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | CARVEDILOL (CARVEDILOL) TABLET, FILM COATED [H.J. HARKINS COMPANY, INC.] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | CARVEDILOL (CARVEDILOL) TABLET, FILM COATED [H.J. HARKINS COMPANY, INC.] | 1 | |
| POLYETHYLENE GLYCOL | INACTIVE INGREDIENT | 3WJQ0SDW1A | CARVEDILOL (CARVEDILOL) TABLET, FILM COATED [H.J. HARKINS COMPANY, INC.] | 1 | |
| POVIDONE | INACTIVE INGREDIENT | FZ989GH94E | CARVEDILOL (CARVEDILOL) TABLET, FILM COATED [H.J. HARKINS COMPANY, INC.] | 1 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | CARVEDILOL (CARVEDILOL) TABLET, FILM COATED [H.J. HARKINS COMPANY, INC.] | 1 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | CARVEDILOL (CARVEDILOL) TABLET, FILM COATED [H.J. HARKINS COMPANY, INC.] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52959-466 | CARVEDILOL (CARVEDILOL) TABLET, FILM COATED [H.J. HARKINS COMPANY, INC.] | 1 | Legacy NDC, 1 package rows | 20111201_ad96f237-1e3a-45ff-9c47-fed3544dc943.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 52959-466-30 | 52959046630 | 30 in 1 BOTTLE | Historical |