Nabumetone
- Product NDC
- 63874-607
- 11-digit product format
- 638740607
- Labeler code
- 63874
- Product ID
- 63874-607_c445da39-f7f2-46a9-871f-a25f1c0f462f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nabumetone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Altura Pharmaceuticals, Inc.
- Application
- ANDA076009
- Marketing category
- ANDA
- Marketing start
- 2010-01-01
- 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 |
|---|
| 63874-607-01 | Nabumetone | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 2 |
| 63874-607-30 | Nabumetone | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 2 |
| 63874-607-60 | Nabumetone | 60 in 1 BOTTLE, PLASTIC | TABLET | 60 | | 2 |
| 63874-607-90 | Nabumetone | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 2 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| NABUMETONE | ACTIVE INGREDIENT | LW0TIW155Z | NABUMETONE TABLET [ALTURA PHARMACEUTICALS, INC.] | 2 | |
| NABUMETONE | ACTIVE MOIETY | LW0TIW155Z | NABUMETONE TABLET [ALTURA PHARMACEUTICALS, INC.] | 2 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | NABUMETONE TABLET [ALTURA PHARMACEUTICALS, INC.] | 2 | |
| COLLOIDAL SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | NABUMETONE TABLET [ALTURA PHARMACEUTICALS, INC.] | 2 | |
| D&C YELLOW NO. 10 | INACTIVE INGREDIENT | 35SW5USQ3G | NABUMETONE TABLET [ALTURA PHARMACEUTICALS, INC.] | 2 | |
| FD&C YELLOW NO. 6 | INACTIVE INGREDIENT | H77VEI93A8 | NABUMETONE TABLET [ALTURA PHARMACEUTICALS, INC.] | 2 | |
| HYPROMELLOSE | INACTIVE INGREDIENT | 3NXW29V3WO | NABUMETONE TABLET [ALTURA PHARMACEUTICALS, INC.] | 2 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | NABUMETONE TABLET [ALTURA PHARMACEUTICALS, INC.] | 2 | |
| POLYETHYLENE GLYCOL | INACTIVE INGREDIENT | 3WJQ0SDW1A | NABUMETONE TABLET [ALTURA PHARMACEUTICALS, INC.] | 2 | |
| POLYSORBATE 80 | INACTIVE INGREDIENT | 6OZP39ZG8H | NABUMETONE TABLET [ALTURA PHARMACEUTICALS, INC.] | 2 | |
| SODIUM LAURYL SULFATE | INACTIVE INGREDIENT | 368GB5141J | NABUMETONE TABLET [ALTURA PHARMACEUTICALS, INC.] | 2 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | NABUMETONE TABLET [ALTURA PHARMACEUTICALS, INC.] | 2 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | NABUMETONE TABLET [ALTURA PHARMACEUTICALS, INC.] | 2 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63874-607 | NABUMETONE TABLET [ALTURA PHARMACEUTICALS, INC.] | 2 | Legacy NDC, 4 package rows | 20100503_e66a5a08-7121-4987-bda1-7f3dbc5ed680.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 63874-607-01 | 63874060701 | 100 in 1 BOTTLE, PLASTIC | Historical |
| 63874-607-30 | 63874060730 | 30 in 1 BOTTLE, PLASTIC | Historical |
| 63874-607-60 | 63874060760 | 60 in 1 BOTTLE, PLASTIC | Historical |
| 63874-607-90 | 63874060790 | 90 in 1 BOTTLE, PLASTIC | Historical |