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"21130-033-53" National Drug Code (NDC)
Famotidine 1 BOTTLE in 1 CARTON (21130-033-53) / 25 TABLET, FILM COATED in 1 BOTTLE
(Better Living Brands, LLC)
NDC Code
21130-033-53
Package Description
1 BOTTLE in 1 CARTON (21130-033-53) / 25 TABLET, FILM COATED in 1 BOTTLE
Product NDC
21130-033
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Famotidine
Non-Proprietary Name
Famotidine
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20230908
Marketing Category Name
ANDA
Application Number
ANDA206531
Manufacturer
Better Living Brands, LLC
Substance Name
FAMOTIDINE
Strength
20
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/21130-033-53