NAPROXEN SODIUM
- Product NDC
- 46994-661
- 11-digit product format
- 469940661
- Labeler code
- 46994
- Product ID
- 46994-661_ee27e839-4bed-2d01-e053-2995a90a82ce
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- NAPROXEN SODIUM
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- SAVE-A-LOT FOOD STORES, LTD.
- Application
- ANDA207612
- Marketing category
- ANDA
- Marketing start
- 2020-03-13
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 46994-661-50 | 46994066150 | 1 BOTTLE in 1 CARTON (46994-661-50) > 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2020-03-13 | 0000-00-00 | No | No | Current |