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"11673-061-02" National Drug Code (NDC)
Up And Up Famotidine 25 BLISTER PACK in 1 CARTON (11673-061-02) > 1 TABLET, FILM COATED in 1 BLISTER PACK
(Target Corporation)
NDC Code
11673-061-02
Package Description
25 BLISTER PACK in 1 CARTON (11673-061-02) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC
11673-061
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Up And Up Famotidine
Non-Proprietary Name
Famotidine
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20120503
Marketing Category Name
ANDA
Application Number
ANDA077351
Manufacturer
Target Corporation
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/11673-061-02