arthritis pain relief

Product NDC
59779-544
11-digit product format
597790544
Labeler code
59779
Product ID
59779-544_cd263063-cac9-4999-afb8-6928cdde3d78
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
CVS Pharmacy
Application
ANDA075077
Marketing category
ANDA
Marketing start
2000-05-31
Marketing end
2019-12-31
Substance
ACETAMINOPHEN
Active strength
650 mg/1
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59779-544-47EA - Each59779-544b49d3270-3650-4db6-bf3c-2d4259c95a3d12018-02-20
59779-544-62EA - Each59779-544659b8e2b-aae8-4233-8324-67a5544a210012018-06-11
59779-544-71EA - Each59779-544d8ce0c90-5a61-4a38-be54-29ce9f1a760a12018-10-11
59779-544-78EA - Each59779-544332ffb01-ef74-4ae5-a02b-b1021ad3c7f512017-11-06