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"37808-302-01" National Drug Code (NDC)
Ranitidine 1 BOTTLE in 1 CARTON (37808-302-01) > 130 TABLET, FILM COATED in 1 BOTTLE
(H-E-B)
NDC Code
37808-302-01
Package Description
1 BOTTLE in 1 CARTON (37808-302-01) > 130 TABLET, FILM COATED in 1 BOTTLE
Product NDC
37808-302
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Ranitidine
Non-Proprietary Name
Ranitidine Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20180124
Marketing Category Name
ANDA
Application Number
ANDA200172
Manufacturer
H-E-B
Substance Name
RANITIDINE HYDROCHLORIDE
Strength
150
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/37808-302-01