Naproxen Sodium
- Product NDC
- 52605-144
- 11-digit product format
- 526050144
- Labeler code
- 52605
- Product ID
- 52605-144_b06d4755-1fbf-4fcf-9075-cb1691292aad
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Polygen Pharmaceuticals LLC
- Application
- ANDA090545
- Marketing category
- ANDA
- Marketing start
- 2012-11-13
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 mg/1
- 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 |
|---|
| 52605-144-01 | Naproxen Sodium | 1 in 1 CARTON | TABLET, COATED | 1 | | 6 |
| 52605-144-01 | Naproxen Sodium | 100 in 1 BOTTLE | TABLET, COATED | 100 | | 6 |
| 52605-144-24 | Naproxen Sodium | 1 in 1 CARTON | TABLET, COATED | 1 | | 6 |
| 52605-144-24 | Naproxen Sodium | 24 in 1 BOTTLE | TABLET, COATED | 24 | | 6 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| NAPROXEN SODIUM | ACTIVE INGREDIENT | 9TN87S3A3C | NAPROXEN SODIUM TABLET, COATED [POLYGEN PHARMACEUTICALS LLC] | 6 | |
| NAPROXEN | ACTIVE MOIETY | 57Y76R9ATQ | NAPROXEN SODIUM TABLET, COATED [POLYGEN PHARMACEUTICALS LLC] | 6 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | NAPROXEN SODIUM TABLET, COATED [POLYGEN PHARMACEUTICALS LLC] | 6 | |
| COLLOIDAL SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | NAPROXEN SODIUM TABLET, COATED [POLYGEN PHARMACEUTICALS LLC] | 6 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | NAPROXEN SODIUM TABLET, COATED [POLYGEN PHARMACEUTICALS LLC] | 6 | |
| FD&C BLUE NO. 2 | INACTIVE INGREDIENT | L06K8R7DQK | NAPROXEN SODIUM TABLET, COATED [POLYGEN PHARMACEUTICALS LLC] | 6 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | NAPROXEN SODIUM TABLET, COATED [POLYGEN PHARMACEUTICALS LLC] | 6 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | NAPROXEN SODIUM TABLET, COATED [POLYGEN PHARMACEUTICALS LLC] | 6 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | NAPROXEN SODIUM TABLET, COATED [POLYGEN PHARMACEUTICALS LLC] | 6 | |
| POVIDONE | INACTIVE INGREDIENT | FZ989GH94E | NAPROXEN SODIUM TABLET, COATED [POLYGEN PHARMACEUTICALS LLC] | 6 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | NAPROXEN SODIUM TABLET, COATED [POLYGEN PHARMACEUTICALS LLC] | 6 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52605-144 | NAPROXEN SODIUM TABLET, COATED [POLYGEN PHARMACEUTICALS LLC] | 6 | Legacy NDC, 4 package rows | 20130626_e8720904-9ac0-46c0-b220-730e373505a7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 52605-144-01 | 52605014401 | 1 in 1 CARTON | Historical |
| 52605-144-24 | 52605014424 | 1 in 1 CARTON | Historical |