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"42708-177-21" National Drug Code (NDC)
Cyproheptadine Hydrochloride 21 TABLET in 1 BOTTLE, PLASTIC (42708-177-21)
(QPharma Inc)
NDC Code
42708-177-21
Package Description
21 TABLET in 1 BOTTLE, PLASTIC (42708-177-21)
Product NDC
42708-177
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Cyproheptadine Hydrochloride
Non-Proprietary Name
Cyproheptadine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20170117
Marketing Category Name
ANDA
Application Number
ANDA206553
Manufacturer
QPharma Inc
Substance Name
CYPROHEPTADINE HYDROCHLORIDE
Strength
4
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/42708-177-21