CareOne Naproxen Sodium
- Product NDC
- 41520-702
- 11-digit product format
- 415200702
- Labeler code
- 41520
- Product ID
- 41520-702_367d0ffa-a7c5-4f6a-9140-83dd1e3b12d6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- American Sales Company
- Application
- ANDA074661
- Marketing category
- ANDA
- Marketing start
- 2021-01-22
- 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 Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41520-702 | CAREONE NAPROXEN SODIUM (NAPROXEN SODIUM) TABLET, FILM COATED [AMERICAN SALES COMPANY] | 4 | Legacy NDC | 20250430_0c9222e0-81e7-4591-b071-14b0e9cbf01e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 41520-702-75 | 41520070275 | 1 BOTTLE in 1 CARTON (41520-702-75) > 90 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2021-12-30 | 0000-00-00 | No | No | Current |
| 41520-702-78 | 41520070278 | 1 BOTTLE in 1 CARTON (41520-702-78) > 100 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2021-01-22 | 0000-00-00 | No | No | Current |