Leader Arthritis Pain Reliever

Product NDC
37205-034
11-digit product format
372050034
Labeler code
37205
Product ID
37205-034_f8bb1520-34d2-4b2c-822b-d9e0d0f90f53
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Cardinal Health
Application
ANDA076200
Marketing category
ANDA
Marketing start
2002-04-30
Marketing end
0000-00-00
Substance
ACETAMINOPHEN
Active strength
650 mg/1
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
37205-034-71EA - Each37205-0341f71898c-92b3-4ab9-a6b9-b76be12c952c12012-07-24
37205-034-78EA - Each37205-03459a0ea53-7601-4e1c-a61a-9dac5daf5bb912012-07-24