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"70436-197-04" National Drug Code (NDC)
Diltiazem Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-197-04)
(Slate Run Pharmaceuticals, LLC)
NDC Code
70436-197-04
Package Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-197-04)
Product NDC
70436-197
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Diltiazem Hydrochloride
Non-Proprietary Name
Diltiazem Hydrochloride
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20230320
Marketing Category Name
ANDA
Application Number
ANDA216439
Manufacturer
Slate Run Pharmaceuticals, LLC
Substance Name
DILTIAZEM HYDROCHLORIDE
Strength
240
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/70436-197-04