Nabumetone
- Product NDC
- 10544-120
- 11-digit product format
- 105440120
- Labeler code
- 10544
- Product ID
- 10544-120_b68c4f58-fe32-4d3b-998a-12e80a1d8432
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nabumetone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Blenheim Pharmacal, Inc.
- Application
- ANDA091083
- Marketing category
- ANDA
- Marketing start
- 2013-05-22
- Marketing end
- 0000-00-00
- Substance
- NABUMETONE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [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 |
|---|
| 10544-120-20 | Nabumetone | 20 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 20 | | 3 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| NABUMETONE | ACTIVE INGREDIENT | LW0TIW155Z | NABUMETONE TABLET, FILM COATED [BLENHEIM PHARMACAL, INC.] | 3 | |
| NABUMETONE | ACTIVE MOIETY | LW0TIW155Z | NABUMETONE TABLET, FILM COATED [BLENHEIM PHARMACAL, INC.] | 3 | |
| COLLOIDAL SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | NABUMETONE TABLET, FILM COATED [BLENHEIM PHARMACAL, INC.] | 3 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | NABUMETONE TABLET, FILM COATED [BLENHEIM PHARMACAL, INC.] | 3 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | NABUMETONE TABLET, FILM COATED [BLENHEIM PHARMACAL, INC.] | 3 | |
| POVIDONE | INACTIVE INGREDIENT | FZ989GH94E | NABUMETONE TABLET, FILM COATED [BLENHEIM PHARMACAL, INC.] | 3 | |
| SODIUM LAURYL SULFATE | INACTIVE INGREDIENT | 368GB5141J | NABUMETONE TABLET, FILM COATED [BLENHEIM PHARMACAL, INC.] | 3 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | NABUMETONE TABLET, FILM COATED [BLENHEIM PHARMACAL, INC.] | 3 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | NABUMETONE TABLET, FILM COATED [BLENHEIM PHARMACAL, INC.] | 3 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | NABUMETONE TABLET, FILM COATED [BLENHEIM PHARMACAL, INC.] | 3 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | NABUMETONE TABLET, FILM COATED [BLENHEIM PHARMACAL, INC.] | 3 | |
| TRIACETIN | INACTIVE INGREDIENT | XHX3C3X673 | NABUMETONE TABLET, FILM COATED [BLENHEIM PHARMACAL, INC.] | 3 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10544-120 | NABUMETONE TABLET, FILM COATED [BLENHEIM PHARMACAL, INC.] | 3 | Legacy NDC, 1 package rows | 20150801_79a0d2b5-2e19-4513-b60c-b612906f0bce.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10544-120-20 | 10544012020 | 20 in 1 BOTTLE, PLASTIC | Historical |