NDC 50090-1327

PREZISTA

Darunavir

PREZISTA is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by A-s Medication Solutions. The primary component is Darunavir Ethan.

Product ID50090-1327_a41f626a-2e4f-43d1-969a-5297cab4271c
NDC50090-1327
Product TypeHuman Prescription Drug
Proprietary NamePREZISTA
Generic NameDarunavir
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2012-11-09
Marketing CategoryNDA / NDA
Application NumberNDA021976
Labeler NameA-S Medication Solutions
Substance NameDARUNAVIR ETHAN
Active Ingredient Strength800 mg/1
Pharm ClassesHIV Protease In
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 50090-1327-0

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-1327-0)
Marketing Start Date2014-11-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50090-1327-0 [50090132700]

PREZISTA TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA021976
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-11-28
Marketing End Date2018-03-31

Drug Details

Active Ingredients

IngredientStrength
DARUNAVIR ETHANOLATE800 mg/1

Pharmacological Class

  • HIV Protease Inhibitors [MoA]
  • Protease Inhibitor [EPC]
  • Cytochrome P450 3A Inhibitors [MoA]
  • Cytochrome P450 2D6 Inhibitors [MoA]

NDC Crossover Matching brand name "PREZISTA" or generic name "Darunavir"

NDCBrand NameGeneric Name
50090-1327PREZISTAdarunavir
50090-1491PREZISTAdarunavir
53808-0672PREZISTAdarunavir ethanolate
53808-0773PREZISTAdarunavir ethanolate
59676-562PREZISTAdarunavir
59676-563PREZISTAdarunavir
59676-564PREZISTAdarunavir
59676-565PREZISTAdarunavir
70518-0689PREZISTAPREZISTA
70518-1483PREZISTAPREZISTA
59676-566PREZISTAPREZISTA

Trademark Results [PREZISTA]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PREZISTA
PREZISTA
78762650 3236346 Live/Registered
JANSSEN SCIENCES IRELAND UNLIMITED COMPANY
2005-11-29
PREZISTA
PREZISTA
77239629 not registered Dead/Abandoned
Tibotec Pharmaceuticals Ltd.
2007-07-26

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