"63304-173-69" National Drug Code (NDC)

Doxycycline 1 BLISTER PACK in 1 CARTON (63304-173-69) > 10 TABLET, FILM COATED in 1 BLISTER PACK (63304-173-11)
(Sun Pharmaceutical Industries Inc.)

NDC Code63304-173-69
Package Description1 BLISTER PACK in 1 CARTON (63304-173-69) > 10 TABLET, FILM COATED in 1 BLISTER PACK (63304-173-11)
Product NDC63304-173
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDoxycycline
Non-Proprietary NameDoxycycline
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180806
Marketing Category NameANDA
Application NumberANDA065356
ManufacturerSun Pharmaceutical Industries Inc.
Substance NameDOXYCYCLINE
Strength150
Strength Unitmg/1
Pharmacy ClassesTetracycline-class Drug [EPC], Tetracyclines [CS]

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