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"16571-805-10" National Drug Code (NDC)
Cyproheptadine Hydrochloride 1000 TABLET in 1 BOTTLE (16571-805-10)
(Rising Pharma Holdings, Inc.)
NDC Code
16571-805-10
Package Description
1000 TABLET in 1 BOTTLE (16571-805-10)
Product NDC
16571-805
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Cyproheptadine Hydrochloride
Non-Proprietary Name
Cyproheptadine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20220209
Marketing Category Name
ANDA
Application Number
ANDA207555
Manufacturer
Rising Pharma Holdings, Inc.
Substance Name
CYPROHEPTADINE HYDROCHLORIDE
Strength
4
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/16571-805-10