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"49348-819-10" National Drug Code (NDC)
Sunmark All Day Relief 1 BOTTLE in 1 CARTON (49348-819-10) > 100 TABLET, FILM COATED in 1 BOTTLE
(McKesson)
NDC Code
49348-819-10
Package Description
1 BOTTLE in 1 CARTON (49348-819-10) > 100 TABLET, FILM COATED in 1 BOTTLE
Product NDC
49348-819
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Sunmark All Day Relief
Non-Proprietary Name
Naproxen Sodium
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20030811
Marketing Category Name
ANDA
Application Number
ANDA074661
Manufacturer
McKesson
Substance Name
NAPROXEN SODIUM
Strength
220
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/49348-819-10