Naproxen Sodium
- Product NDC
- 70677-1148
- 11-digit product format
- 706771148
- Labeler code
- 70677
- Product ID
- 70677-1148_24b5df2d-bb93-4790-b72b-cb7d0f617f4e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- ANDA208363
- Marketing category
- ANDA
- Marketing start
- 2023-03-31
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 9TN87S3A3C | NAPROXEN SODIUM | 26159-34-2 | NAPROXEN SODIUM |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 70677-1148-1 | 70677114801 | 1 BOTTLE, PLASTIC in 1 BOX (70677-1148-1) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2023-03-31 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Drug Facts | Strategic Sourcing Services LLC | 2023-10-02 | HUMAN OTC DRUG LABEL | 2 |