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"0093-0321-01" National Drug Code (NDC)
Diltiazem Hydrochloride 100 TABLET, FILM COATED in 1 BOTTLE (0093-0321-01)
(Teva Pharmaceuticals USA, Inc.)
NDC Code
0093-0321-01
Package Description
100 TABLET, FILM COATED in 1 BOTTLE (0093-0321-01)
Product NDC
0093-0321
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
19951226
Marketing Category Name
ANDA
Application Number
ANDA074185
Manufacturer
Teva Pharmaceuticals USA, Inc.
Substance Name
DILTIAZEM HYDROCHLORIDE
Strength
120
Strength Unit
mg/1
Pharmacy Classes
Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0093-0321-01