Arthritis Pain

Product NDC
68998-300
11-digit product format
689980300
Labeler code
68998
Product ID
68998-300_bccb55cc-368a-54a0-e053-2a95a90ad8eb
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
MARC GLASSMAN, INC.
Application
ANDA211544
Marketing category
ANDA
Marketing start
2020-03-31
Marketing end
0000-00-00
Substance
ACETAMINOPHEN
Active strength
650 mg/1
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68998-300ARTHRITIS PAIN (ACETAMINOPHEN) TABLET, EXTENDED RELEASE [MARC GLASSMAN, INC.]3Legacy NDC20241207_951be9e6-8c5d-3c8f-e053-2995a90a462f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
68998-300-03689980300031 BOTTLE, PLASTIC in 1 CARTON (68998-300-03) > 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC2020-03-310000-00-00NoNoCurrent