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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0143-9916-01EA - Each0143-99165986ee50-bcc4-414a-a92b-df039426ddb512013-05-02