Naproxen Sodium 220mg
- Product NDC
- 53185-362
- 11-digit product format
- 531850362
- Labeler code
- 53185
- Product ID
- 53185-362_15a4708b-ad90-4051-9b5d-976f70658931
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium 220mg
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Athlete's Needs, Inc.
- Application
- ANDA090545
- Marketing category
- ANDA
- Marketing start
- 2014-12-23
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 53185-362-50 | Naproxen Sodium 220mg | 50 in 1 BOTTLE | TABLET, COATED | 50 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53185-362 | NAPROXEN SODIUM 220MG TABLET, COATED [ATHLETE'S NEEDS, INC.] | 4 | Legacy NDC, 1 package rows | 20210422_91e1fef2-0e9b-4553-92f2-ddf219990695.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 |
|---|
| 53185-362-50 | 53185036250 | 50 TABLET, COATED in 1 BOTTLE (53185-362-50) | 2014-12-23 | 0000-00-00 | No | No | Current |