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"49348-921-10" National Drug Code (NDC)
Sunmark Arthritis Pain Reliever 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (49348-921-10)
(Sunmark)
NDC Code
49348-921-10
Package Description
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (49348-921-10)
Product NDC
49348-921
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Sunmark Arthritis Pain Reliever
Non-Proprietary Name
Acetaminophen
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20020430
Marketing Category Name
ANDA
Application Number
ANDA076200
Manufacturer
Sunmark
Substance Name
ACETAMINOPHEN
Strength
650
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/49348-921-10