"49349-242-02" National Drug Code (NDC)

Diltiazem Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (49349-242-02)
(REMEDYREPACK INC.)

NDC Code49349-242-02
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (49349-242-02)
Product NDC49349-242
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDiltiazem Hydrochloride
Non-Proprietary NameDiltiazem Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20091119
Marketing Category NameANDA
Application NumberANDA072838
ManufacturerREMEDYREPACK INC.
Substance NameDILTIAZEM HYDROCHLORIDE
Strength60
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

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