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"69306-266-30" National Drug Code (NDC)
Ibuprofen And Famotidine 30 TABLET, FILM COATED in 1 BOTTLE (69306-266-30)
(Doc Rx)
NDC Code
69306-266-30
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (69306-266-30)
Product NDC
69306-266
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ibuprofen And Famotidine
Non-Proprietary Name
Ibuprofen And Famotidine
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20210804
Marketing Category Name
ANDA
Application Number
ANDA211890
Manufacturer
Doc Rx
Substance Name
FAMOTIDINE; IBUPROFEN
Strength
26.6; 800
Strength Unit
mg/1; mg/1
Pharmacy Classes
Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/69306-266-30