NABUMETONE
- Product NDC
- 61919-698
- 11-digit product format
- 619190698
- Labeler code
- 61919
- Product ID
- 61919-698_90a2e268-bee7-498d-e053-2995a90ad52b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- NABUMETONE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA078671
- Marketing category
- ANDA
- Marketing start
- 2019-08-21
- 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
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 |
|---|
| 61919-698-30 | NABUMETONE | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 1 |
| 61919-698-60 | NABUMETONE | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-698 | NABUMETONE TABLET, FILM COATED [DIRECT_RX] | 1 | Legacy NDC, 1 package rows | 20190823_90b6d62f-6684-73bc-e053-2995a90a1a75.zip |
| 61919-698 | NABUMETONE TABLET, FILM COATED [DIRECT_RX] | 1 | Legacy NDC, 1 package rows | 20190822_90a2e268-bee6-498d-e053-2995a90ad52b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-698-30 | 61919069830 | 30 TABLET, FILM COATED in 1 BOTTLE (61919-698-30) | 2019-08-21 | 0000-00-00 | No | No | Current |
| 61919-698-60 | 61919069860 | 60 TABLET, FILM COATED in 1 BOTTLE (61919-698-60) | 2019-08-22 | 0000-00-00 | No | No | Current |