Good Sense Naproxen Sodium
- Product NDC
- 50090-3369
- 11-digit product format
- 500903369
- Labeler code
- 50090
- Product ID
- 50090-3369_eca9b79c-1ce0-4be3-9c50-c4c2669e3283
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA074661
- Marketing category
- ANDA
- Marketing start
- 2014-03-31
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 50090-3369-0 | Good Sense Naproxen Sodium | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3369 | GOOD SENSE NAPROXEN SODIUM (NAPROXEN SODIUM) TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 1 | Legacy NDC, 1 package rows | 20190205_494db9ba-6907-497d-a150-451e12c81cb1.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 |
|---|
| 50090-3369-0 | 50090336900 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-3369-0) | 2018-02-12 | 0000-00-00 | No | No | Current |