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"68084-984-32" National Drug Code (NDC)
Ranitidine 20 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-984-32) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-984-33)
(American Health Packaging)
NDC Code
68084-984-32
Package Description
20 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-984-32) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-984-33)
Product NDC
68084-984
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ranitidine
Non-Proprietary Name
Ranitidine
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20150331
Marketing Category Name
ANDA
Application Number
ANDA078542
Manufacturer
American Health Packaging
Substance Name
RANITIDINE HYDROCHLORIDE
Strength
300
Strength Unit
mg/1
Pharmacy Classes
Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68084-984-32