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"55111-131-81" National Drug Code (NDC)
Ranitidine 3 BLISTER PACK in 1 CARTON (55111-131-81) > 10 TABLET in 1 BLISTER PACK
(Dr. Reddy's Laboratories Limited)
NDC Code
55111-131-81
Package Description
3 BLISTER PACK in 1 CARTON (55111-131-81) > 10 TABLET in 1 BLISTER PACK
Product NDC
55111-131
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Ranitidine
Non-Proprietary Name
Ranitidine
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20000301
Marketing Category Name
ANDA
Application Number
ANDA075294
Manufacturer
Dr. Reddy's Laboratories Limited
Substance Name
RANITIDINE HYDROCHLORIDE
Strength
75
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/55111-131-81