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"16571-772-09" National Drug Code (NDC)
Fosinopril Sodium 90 TABLET in 1 BOTTLE (16571-772-09)
(Rising Pharma Holdings, Inc.)
NDC Code
16571-772-09
Package Description
90 TABLET in 1 BOTTLE (16571-772-09)
Product NDC
16571-772
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fosinopril Sodium
Non-Proprietary Name
Fosinopril Sodium
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20110330
Marketing Category Name
ANDA
Application Number
ANDA091163
Manufacturer
Rising Pharma Holdings, Inc.
Substance Name
FOSINOPRIL SODIUM
Strength
40
Strength Unit
mg/1
Pharmacy Classes
Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/16571-772-09