naproxen sodium
- Product NDC
- 11822-0507
- 11-digit product format
- 118220507
- Labeler code
- 11822
- Product ID
- 11822-0507_54e97657-b9ef-48e4-9fd5-945a98d0b92a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Rite Aid Corporation
- Application
- ANDA074661
- Marketing category
- ANDA
- Marketing start
- 2001-05-16
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| NAPROXEN SODIUM | ACTIVE INGREDIENT | 9TN87S3A3C | NAPROXEN SODIUM TABLET, FILM COATED [RITE AID CORPORATION] | 3 | |
| NAPROXEN | ACTIVE MOIETY | 57Y76R9ATQ | NAPROXEN SODIUM TABLET, FILM COATED [RITE AID CORPORATION] | 3 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | NAPROXEN SODIUM TABLET, FILM COATED [RITE AID CORPORATION] | 3 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | NAPROXEN SODIUM TABLET, FILM COATED [RITE AID CORPORATION] | 3 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | NAPROXEN SODIUM TABLET, FILM COATED [RITE AID CORPORATION] | 3 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | NAPROXEN SODIUM TABLET, FILM COATED [RITE AID CORPORATION] | 3 | |
| POVIDONES | INACTIVE INGREDIENT | FZ989GH94E | NAPROXEN SODIUM TABLET, FILM COATED [RITE AID CORPORATION] | 3 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | NAPROXEN SODIUM TABLET, FILM COATED [RITE AID CORPORATION] | 3 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | NAPROXEN SODIUM TABLET, FILM COATED [RITE AID CORPORATION] | 3 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11822-0507 | NAPROXEN SODIUM TABLET, FILM COATED [RITE AID CORPORATION] | 7 | Legacy NDC | 20221112_af07cecf-e8f5-4f76-9df7-e634256f332f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-0507-1 | 11822050701 | 1 BOTTLE in 1 CARTON (11822-0507-1) > 50 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2001-06-25 | 0000-00-00 | No | No | Current |
| 11822-0507-2 | 11822050702 | 1 BOTTLE in 1 CARTON (11822-0507-2) > 120 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2005-12-06 | 0000-00-00 | No | No | Current |
| 11822-0507-3 | 11822050703 | 1 BOTTLE in 1 CARTON (11822-0507-3) > 24 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2014-05-28 | 0000-00-00 | No | No | Current |
| 11822-0507-7 | 11822050707 | 1 BOTTLE in 1 CARTON (11822-0507-7) > 100 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2001-05-16 | 0000-00-00 | No | No | Current |
| 11822-0507-8 | 11822050708 | 1 BOTTLE in 1 CARTON (11822-0507-8) > 200 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2001-05-31 | 0000-00-00 | No | No | Current |
| 11822-0507-9 | 11822050709 | 1 BOTTLE in 1 CARTON (11822-0507-9) > 90 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2022-01-17 | 0000-00-00 | No | No | Current |