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"11673-835-06" National Drug Code (NDC)
Up And Up Ibuprofen Sodium 1 BOTTLE in 1 CARTON (11673-835-06) > 160 TABLET, FILM COATED in 1 BOTTLE
(Target Corporation)
NDC Code
11673-835-06
Package Description
1 BOTTLE in 1 CARTON (11673-835-06) > 160 TABLET, FILM COATED in 1 BOTTLE
Product NDC
11673-835
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Up And Up Ibuprofen Sodium
Non-Proprietary Name
Ibuprofen
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20170302
Marketing Category Name
ANDA
Application Number
ANDA206581
Manufacturer
Target Corporation
Substance Name
IBUPROFEN SODIUM
Strength
256
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/11673-835-06