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"51660-352-69" National Drug Code (NDC)
Acid Reducer 1 BLISTER PACK in 1 CARTON (51660-352-69) > 10 TABLET, FILM COATED in 1 BLISTER PACK
(Ohm Laboratories Inc.)
NDC Code
51660-352-69
Package Description
1 BLISTER PACK in 1 CARTON (51660-352-69) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC
51660-352
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Acid Reducer
Non-Proprietary Name
Ranitidine Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20120710
Marketing Category Name
ANDA
Application Number
ANDA201745
Manufacturer
Ohm Laboratories Inc.
Substance Name
RANITIDINE HYDROCHLORIDE
Strength
75
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51660-352-69