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"70677-0019-1" National Drug Code (NDC)
Sunmark Arthritis Pain Reliever 1 BOTTLE in 1 CARTON (70677-0019-1) > 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
(Strategic Sourcing Services LLC)
NDC Code
70677-0019-1
Package Description
1 BOTTLE in 1 CARTON (70677-0019-1) > 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product NDC
70677-0019
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
20170526
Marketing Category Name
ANDA
Application Number
ANDA075077
Manufacturer
Strategic Sourcing Services LLC
Substance Name
ACETAMINOPHEN
Strength
650
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70677-0019-1