All Day Pain Relief
- Product NDC
- 59428-604
- 11-digit product format
- 594280604
- Labeler code
- 59428
- Product ID
- 59428-604_9d429a1c-a5e0-4739-80a5-d3c39ef7a764
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Zapotol Products Corp
- Application
- ANDA204872
- Marketing category
- ANDA
- Marketing start
- 2020-10-22
- 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- All Day Pain Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| NAPROXEN SODIUM | 220 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9TN87S3A3C |
| Rxcui | 849574 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59428-604-08 | All Day Pain Relief | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 1 |
| 59428-604-08 | All Day Pain Relief | 24 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 24 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 59428-604-08 | 59428060408 | 1 BOTTLE, PLASTIC in 1 CARTON (59428-604-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 2020-10-22 | No | No | Historical |