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"53808-0776-1" National Drug Code (NDC)
Ranitidine Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (53808-0776-1)
(State of Florida DOH Central Pharmacy)
NDC Code
53808-0776-1
Package Description
30 TABLET, FILM COATED in 1 BLISTER PACK (53808-0776-1)
Product NDC
53808-0776
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ranitidine Hydrochloride
Non-Proprietary Name
Ranitidine Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20090701
Marketing Category Name
ANDA
Application Number
ANDA074467
Manufacturer
State of Florida DOH Central Pharmacy
Substance Name
RANITIDINE HYDROCHLORIDE
Strength
150
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/53808-0776-1