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"37808-490-71" National Drug Code (NDC)
Rx Act All Day Pain Relief 1 BOTTLE in 1 CARTON (37808-490-71) > 50 TABLET in 1 BOTTLE
(H E B)
NDC Code
37808-490-71
Package Description
1 BOTTLE in 1 CARTON (37808-490-71) > 50 TABLET in 1 BOTTLE
Product NDC
37808-490
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Rx Act All Day Pain Relief
Non-Proprietary Name
Naproxen Sodium
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
19970224
Marketing Category Name
ANDA
Application Number
ANDA074661
Manufacturer
H E B
Substance Name
NAPROXEN SODIUM
Strength
220
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/37808-490-71