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"70436-200-04" National Drug Code (NDC)

Diltiazem Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-200-04)
(Slate Run Pharmaceuticals, LLC)

NDC Code70436-200-04
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-200-04)
Product NDC70436-200
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDiltiazem Hydrochloride
Non-Proprietary NameDiltiazem Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20230320
Marketing Category NameANDA
Application NumberANDA216439
ManufacturerSlate Run Pharmaceuticals, LLC
Substance NameDILTIAZEM HYDROCHLORIDE
Strength420
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A4 Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70436-200-04





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