"49349-315-02" National Drug Code (NDC)

Labetalol Hydrochloride 30 TABLET in 1 BLISTER PACK (49349-315-02)
(REMEDYREPACK INC.)

NDC Code49349-315-02
Package Description30 TABLET in 1 BLISTER PACK (49349-315-02)
Product NDC49349-315
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20110620
Marketing Category NameANDA
Application NumberANDA074787
ManufacturerREMEDYREPACK INC.
Substance NameLABETALOL HYDROCHLORIDE
Strength300
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

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