Nabumetone
- Product NDC
- 55700-765
- 11-digit product format
- 557000765
- Labeler code
- 55700
- Product ID
- 55700-765_f89a80ff-b6ac-4818-95e1-43bd1d58fc9e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nabumetone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA075189
- Marketing category
- ANDA
- Marketing start
- 2019-06-14
- Marketing end
- 0000-00-00
- Substance
- NABUMETONE
- Active strength
- 750 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 55700-765-30 | 2025-01-10 | C162847 | 48780-1 | ba0f9c33-2872-a910-e053-dadaa90a0b85 | cab5d1e7-1940-4d0d-9b7c-d6d422f39152 |
| 55700-765-60 | 2025-01-10 | C162847 | 48780-1 | ba0f9c33-2872-a910-e053-dadaa90a0b85 | cab5d1e7-1940-4d0d-9b7c-d6d422f39152 |
| 55700-765-30 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-2872-a910-e053-dadaa90a0b85 | cab5d1e7-1940-4d0d-9b7c-d6d422f39152 |
| 55700-765-60 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-2872-a910-e053-dadaa90a0b85 | cab5d1e7-1940-4d0d-9b7c-d6d422f39152 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 55700-765-30 | EA - Each | 55700-765 | d8361900-b25c-415d-8b66-ae88dd830e93 | 1 | 2019-07-02 |
| 55700-765-60 | EA - Each | 55700-765 | 258aba53-df3a-4b01-a0af-7e7a78fbe120 | 1 | 2019-10-07 |