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"51672-2115-2" National Drug Code (NDC)
Feverall 6 BLISTER PACK in 1 CARTON (51672-2115-2) > 1 SUPPOSITORY in 1 BLISTER PACK (51672-2115-0)
(Taro Pharmaceuticals U.S.A. Inc.)
NDC Code
51672-2115-2
Package Description
6 BLISTER PACK in 1 CARTON (51672-2115-2) > 1 SUPPOSITORY in 1 BLISTER PACK (51672-2115-0)
Product NDC
51672-2115
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Feverall
Proprietary Name Suffix
Childrens
Non-Proprietary Name
Acetaminophen
Dosage Form
SUPPOSITORY
Usage
RECTAL
Start Marketing Date
20131212
Marketing Category Name
NDA
Application Number
NDA018337
Manufacturer
Taro Pharmaceuticals U.S.A. Inc.
Substance Name
ACETAMINOPHEN
Strength
120
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51672-2115-2