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"70518-0109-1" National Drug Code (NDC)
Diltiazem Hydrochloride 100 POUCH in 1 BOX (70518-0109-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-0109-2)
(REMEDYREPACK INC.)
NDC Code
70518-0109-1
Package Description
100 POUCH in 1 BOX (70518-0109-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-0109-2)
Product NDC
70518-0109
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
20170109
Marketing Category Name
ANDA
Application Number
ANDA074185
Manufacturer
REMEDYREPACK INC.
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/70518-0109-1