Nabumetone
- Product NDC
- 53217-260
- 11-digit product format
- 532170260
- Labeler code
- 53217
- Product ID
- 53217-260_8a91200a-ff22-4e06-804d-4f18d355c164
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nabumetone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aidarex Pharmaceuticals LLC
- Application
- ANDA078671
- Marketing category
- ANDA
- Marketing start
- 2015-04-14
- Marketing end
- 0000-00-00
- Substance
- NABUMETONE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 53217-260-30 | Nabumetone | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 1 |
| 53217-260-60 | Nabumetone | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 1 |
| 53217-260-90 | Nabumetone | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53217-260 | NABUMETONE TABLET, FILM COATED [AIDAREX PHARMACEUTICALS LLC] | 1 | Legacy NDC, 3 package rows | 20170420_1bbca935-fa07-44f3-b324-de3961b9fe4c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 53217-260-30 | 53217026030 | 30 in 1 BOTTLE | Historical |
| 53217-260-60 | 53217026060 | 60 in 1 BOTTLE | Historical |
| 53217-260-90 | 53217026090 | 90 in 1 BOTTLE | Historical |