FDA.reportPublic FDA data

Application 084768

Type
ANDA
Sponsor
BARR

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001CHLORDIAZEPOXIDE HYDROCHLORIDECHLORDIAZEPOXIDE HYDROCHLORIDECAPSULE;ORAL5MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
0555-0158Chlordiazepoxide HydrochlorideChlordiazepoxide HydrochlorideTeva Pharmaceuticals USA, Inc.ANDACurrent
0555-0158Chlordiazepoxide HydrochlorideChlordiazepoxide HydrochlorideTeva Pharmaceuticals USA, Inc.ANDACurrent
0555-0158Chlordiazepoxide HydrochlorideChlordiazepoxide HydrochlorideTeva Pharmaceuticals USA, Inc.ANDACurrent
0555-0158Chlordiazepoxide HydrochlorideChlordiazepoxide HydrochlorideTeva Pharmaceuticals USA, Inc.ANDACurrent
0555-0158Chlordiazepoxide HydrochlorideChlordiazepoxide HydrochlorideTeva Pharmaceuticals USA, Inc.ANDACurrent
0555-0158Chlordiazepoxide HydrochlorideChlordiazepoxide HydrochlorideTeva Pharmaceuticals USA, Inc.ANDACurrent
51079-374Chlordiazepoxide HydrochlorideChlordiazepoxide HydrochlorideMylan Institutional Inc.ANDACurrent
51079-374Chlordiazepoxide HydrochlorideChlordiazepoxide HydrochlorideMylan Institutional Inc.ANDACurrent
51079-374Chlordiazepoxide HydrochlorideChlordiazepoxide HydrochlorideMylan Institutional Inc.ANDACurrent
51079-374Chlordiazepoxide HydrochlorideChlordiazepoxide HydrochlorideMylan Institutional Inc.ANDACurrent
67046-396Chlordiazepoxide HydrochlorideChlordiazepoxide HydrochlorideCoupler Enterprises Inc.ANDACurrent
70518-3134Chlordiazepoxide HydrochlorideChlordiazepoxide HydrochlorideREMEDYREPACK INC.ANDACurrent