Naproxen
- Product NDC
- 10544-939
- 11-digit product format
- 105440939
- Labeler code
- 10544
- Product ID
- 10544-939_26a262b0-d022-1e35-e054-00144ff8d46c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Naproxen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Blenheim Pharmacal, Inc.
- Application
- ANDA091305
- Marketing category
- ANDA
- Marketing start
- 2015-07-06
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN
- Active strength
- 500 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
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 |
|---|
| 10544-939-14 | Naproxen | 14 in 1 BOTTLE | TABLET | 14 | | 3 |
| 10544-939-30 | Naproxen | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10544-939 | NAPROXEN TABLET [BLENHEIM PHARMACAL, INC.] | 3 | Legacy NDC, 2 package rows | 20151211_1a374a88-934a-5e61-e054-00144ff88e88.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10544-939-14 | 10544093914 | 14 in 1 BOTTLE | Historical |
| 10544-939-30 | 10544093930 | 30 in 1 BOTTLE | Historical |