NAPROXEN
- Product NDC
- 70518-2428
- 11-digit product format
- 705182428
- Labeler code
- 70518
- Product ID
- 70518-2428_c935bb3c-d8af-8ef2-e053-2995a90a661d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- NAPROXEN
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA091416
- Marketing category
- ANDA
- Marketing start
- 2019-11-18
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 70518-2428-0 | 70518242800 | 30 TABLET in 1 BLISTER PACK (70518-2428-0) | 30 tablet | 2019-11-18 | 0000-00-00 | No | No | Current |