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"37808-050-60" National Drug Code (NDC)
Rx Act Ibuprofen Pm 1 BOTTLE in 1 CARTON (37808-050-60) > 20 TABLET, COATED in 1 BOTTLE
(H E B)
NDC Code
37808-050-60
Package Description
1 BOTTLE in 1 CARTON (37808-050-60) > 20 TABLET, COATED in 1 BOTTLE
Product NDC
37808-050
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Rx Act Ibuprofen Pm
Non-Proprietary Name
Diphenhydramine Citrate, Ibuprofen
Dosage Form
TABLET, COATED
Usage
ORAL
Start Marketing Date
20090311
Marketing Category Name
ANDA
Application Number
ANDA079113
Manufacturer
H E B
Substance Name
DIPHENHYDRAMINE CITRATE; IBUPROFEN
Strength
38; 200
Strength Unit
mg/1; mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/37808-050-60