"49349-258-02" National Drug Code (NDC)

Flomax 30 CAPSULE in 1 BLISTER PACK (49349-258-02)
(REMEDYREPACK INC.)

NDC Code49349-258-02
Package Description30 CAPSULE in 1 BLISTER PACK (49349-258-02)
Product NDC49349-258
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFlomax
Non-Proprietary NameFlomax
Dosage FormCAPSULE
UsageORAL
Start Marketing Date20110330
Marketing Category NameNDA
Application NumberNDA020579
ManufacturerREMEDYREPACK INC.
Substance NameTAMSULOSIN HYDROCHLORIDE
Strength.4
Strength Unitmg/1
Pharmacy ClassesAdrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]

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