NAPROXEN
- Product NDC
- 0143-9916
- 11-digit product format
- 001439916
- Labeler code
- 0143
- Product ID
- 0143-9916_9dee0114-306a-44d3-9b05-e8b033ca24f6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- naproxen sodium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- West-Ward Pharmaceuticals Corp
- Application
- ANDA074480
- Marketing category
- ANDA
- Marketing start
- 1998-02-18
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN SODIUM
- Active strength
- 275 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record