Nabumetone
- Product NDC
- 52959-656
- 11-digit product format
- 529590656
- Labeler code
- 52959
- Product ID
- 52959-656_0ebcf6fc-a0cf-491d-b833-42ac160dc5e0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nabumetone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- H.J. Harkins Company, Inc.
- Application
- ANDA078671
- Marketing category
- ANDA
- Marketing start
- 2008-03-01
- Marketing end
- 0000-00-00
- Substance
- NABUMETONE
- Active strength
- 750 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 52959-656-02 | EA - Each | 52959-656 | 5ac475a6-1bbc-45fa-afe4-96c7c40bec27 | 1 | 2013-02-13 |
| 52959-656-20 | EA - Each | 52959-656 | ef716ad9-3826-4bb2-bbdf-bc642d8da943 | 1 | 2012-07-24 |
| 52959-656-28 | EA - Each | 52959-656 | a71bdb14-c95d-48a2-aaf2-b14f2a1b1932 | 1 | 2012-07-24 |
| 52959-656-30 | EA - Each | 52959-656 | e733adea-7665-4785-bebe-4778c54159e6 | 1 | 2012-07-24 |
| 52959-656-40 | EA - Each | 52959-656 | 31a8996b-0549-49c1-9ee7-e69e232a8f45 | 1 | 2012-07-24 |
| 52959-656-42 | EA - Each | 52959-656 | 6738022b-7570-4383-a207-aceff2c68320 | 1 | 2012-07-24 |
| 52959-656-60 | EA - Each | 52959-656 | f8b07cf9-d643-4711-8bb7-0c8139ca158f | 1 | 2012-07-24 |
| 52959-656-90 | EA - Each | 52959-656 | 68f9c98a-35d1-42d2-ac69-943f2d3a7b40 | 1 | 2012-07-24 |