Pain and Fever Relief
- Product NDC
- 72090-003
- 11-digit product format
- 720900003
- Labeler code
- 72090
- Product ID
- 72090-003_c29fe377-2308-9b47-e053-2995a90a3846
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Pioneer Life Sciences, LLC
- Application
- ANDA207612
- Marketing category
- ANDA
- Marketing start
- 2021-05-19
- 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 |
|---|
| 72090-003-01 | Pain and Fever Relief | 300 in 1 BOTTLE | TABLET | 300 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72090-003 | PAIN AND FEVER RELIEF (NAPROXEN SODIUM) TABLET [PIONEER LIFE SCIENCES, LLC] | 1 | Legacy NDC, 1 package rows | 20210520_c29fec0c-a858-ef95-e053-2995a90a81d8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72090-003-01 | 72090000301 | 300 TABLET in 1 BOTTLE (72090-003-01) | 300 tablet | 2021-05-19 | 0000-00-00 | No | No | Current |