Naproxen
- Product NDC
- 63629-6657
- 11-digit product format
- 636296657
- Labeler code
- 63629
- Product ID
- 63629-6657_8dbc4051-330c-4c87-a7a1-b9aa12d7c1c8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Naproxen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078250
- Marketing category
- ANDA
- Marketing start
- 2007-07-01
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6657-1 | 63629665701 | 20 TABLET in 1 BOTTLE (63629-6657-1) | 20 tablet | 2015-08-10 | 0000-00-00 | No | No | Current |
| 63629-6657-2 | 63629665702 | 30 TABLET in 1 BOTTLE (63629-6657-2) | 30 tablet | 2015-08-10 | 0000-00-00 | No | No | Current |
| 63629-6657-3 | 63629665703 | 60 TABLET in 1 BOTTLE (63629-6657-3) | 60 tablet | 2015-08-10 | 0000-00-00 | No | No | Current |