FDA.reportPublic FDA data

Application 073037

Type
ANDA
Sponsor
PHARM ASSOC

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001HALOPERIDOLHALOPERIDOL LACTATECONCENTRATE;ORALEQ 2MG BASE/MLNoYes

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
0121-0581HaloperidolHaloperidolPharmaceutical Associates, Inc.ANDACurrent
0121-0581HaloperidolHaloperidolPharmaceutical Associates, Inc.ANDACurrent
0121-0581HaloperidolHaloperidolPharmaceutical Associates, Inc.ANDACurrent
0121-0581HaloperidolHaloperidolPharmaceutical Associates, Inc.ANDACurrent
0121-0581HaloperidolHaloperidolPharmaceutical Associates, Inc.ANDACurrent
0121-0581HaloperidolHaloperidolPharmaceutical Associates, Inc.ANDACurrent
0121-0581HaloperidolHaloperidolPharmaceutical Associates, Inc.ANDACurrent
17856-0581HaloperidolHaloperidolAtlantic Biologicals CorpsANDACurrent