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"11673-210-62" National Drug Code (NDC)
Up And Up Arthritis Pain Relief 1 BOTTLE in 1 CARTON (11673-210-62) > 24 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
(Target Corporation)
NDC Code
11673-210-62
Package Description
1 BOTTLE in 1 CARTON (11673-210-62) > 24 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product NDC
11673-210
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Up And Up Arthritis Pain Relief
Non-Proprietary Name
Acetaminophen
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20150306
End Marketing Date
20211130
Marketing Category Name
ANDA
Application Number
ANDA075077
Manufacturer
Target Corporation
Substance Name
ACETAMINOPHEN
Strength
650
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/11673-210-62