Naproxen
- Product NDC
- 67296-0708
- 11-digit product format
- 672960708
- Labeler code
- 67296
- Product ID
- 67296-0708_9c9ae05a-bcbd-79b6-e053-2a95a90a88ca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Naproxen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA074201
- Marketing category
- ANDA
- Marketing start
- 1993-12-22
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN
- 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
- 2021-12-31
- 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 |
|---|
| 67296-0708-1 | Naproxen | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
| 67296-0708-2 | Naproxen | 60 in 1 BOTTLE | TABLET | 60 | | 3 |
| 67296-0708-3 | Naproxen | 20 in 1 BOTTLE | TABLET | 20 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-0708 | NAPROXEN TABLET [REDPHARM DRUG, INC.] | 3 | Legacy NDC, 3 package rows | 20200121_415eb16c-2064-2ec7-e054-00144ff88e88.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67296-0708-1 | 67296070801 | 30 TABLET in 1 BOTTLE (67296-0708-1) | 30 tablet | 1993-12-22 | 0000-00-00 | No | No | Current |
| 67296-0708-2 | 67296070802 | 60 TABLET in 1 BOTTLE (67296-0708-2) | 60 tablet | 1993-12-22 | 0000-00-00 | No | No | Current |
| 67296-0708-3 | 67296070803 | 20 TABLET in 1 BOTTLE (67296-0708-3) | 20 tablet | 1993-12-22 | 0000-00-00 | No | No | Current |