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"70771-1932-5" National Drug Code (NDC)
Diltiazem Hydrochloride 500 TABLET in 1 BOTTLE (70771-1932-5)
(Zydus Lifesciences Limited)
NDC Code
70771-1932-5
Package Description
500 TABLET in 1 BOTTLE (70771-1932-5)
Product NDC
70771-1932
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Diltiazem Hydrochloride
Non-Proprietary Name
Diltiazem Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20260525
Marketing Category Name
ANDA
Application Number
ANDA219253
Manufacturer
Zydus Lifesciences Limited
Substance Name
DILTIAZEM HYDROCHLORIDE
Strength
120
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/70771-1932-5