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"0069-0121-02" National Drug Code (NDC)
Famotidine 25 VIAL, SINGLE-DOSE in 1 CARTON (0069-0121-02) > 2 mL in 1 VIAL, SINGLE-DOSE (0069-0121-01)
(Pfizer Laboratories Div Pfizer Inc)
NDC Code
0069-0121-02
Package Description
25 VIAL, SINGLE-DOSE in 1 CARTON (0069-0121-02) > 2 mL in 1 VIAL, SINGLE-DOSE (0069-0121-01)
Product NDC
0069-0121
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Famotidine
Non-Proprietary Name
Famotidine
Dosage Form
INJECTION, SOLUTION
Usage
INTRAVENOUS
Start Marketing Date
20110510
Marketing Category Name
ANDA
Application Number
ANDA078642
Manufacturer
Pfizer Laboratories Div Pfizer Inc
Substance Name
FAMOTIDINE
Strength
10
Strength Unit
mg/mL
Pharmacy Classes
Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0069-0121-02