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"60687-717-01" National Drug Code (NDC)
Diltiazem Hydrochloride 100 BLISTER PACK in 1 CARTON (60687-717-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-717-11)
(American Health Packaging)
NDC Code
60687-717-01
Package Description
100 BLISTER PACK in 1 CARTON (60687-717-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-717-11)
Product NDC
60687-717
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Diltiazem Hydrochloride
Non-Proprietary Name
Diltiazem Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20230327
Marketing Category Name
ANDA
Application Number
ANDA074185
Manufacturer
American Health Packaging
Substance Name
DILTIAZEM HYDROCHLORIDE
Strength
30
Strength Unit
mg/1
Pharmacy Classes
Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A4 Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/60687-717-01