NDC 63304-086

droxidopa

Droxidopa

droxidopa is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Sun Pharmaceutical Industries, Inc.. The primary component is Droxidopa.

Product ID63304-086_ca97f06d-5449-4f4f-a362-47f65448bf8c
NDC63304-086
Product TypeHuman Prescription Drug
Proprietary Namedroxidopa
Generic NameDroxidopa
Dosage FormCapsule
Route of AdministrationORAL
Marketing Start Date2021-02-18
Marketing CategoryANDA /
Application NumberANDA214384
Labeler NameSun Pharmaceutical Industries, Inc.
Substance NameDROXIDOPA
Active Ingredient Strength100 ug/1
Pharm ClassesCatecholamines [CS],Increased Blood Pressure [PE]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 63304-086-90

90 CAPSULE in 1 BOTTLE (63304-086-90)
Marketing Start Date2021-02-18
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "droxidopa" or generic name "Droxidopa"

NDCBrand NameGeneric Name
0054-0532DroxidopaDroxidopa
0054-0533DroxidopaDroxidopa
0054-0534DroxidopaDroxidopa
0832-0720DroxidopaDroxidopa
0832-0721DroxidopaDroxidopa
0832-0722DroxidopaDroxidopa
27241-199DroxidopaDroxidopa
27241-200DroxidopaDroxidopa
27241-201DroxidopaDroxidopa
27808-199droxidopadroxidopa
27808-200droxidopadroxidopa
27808-201droxidopadroxidopa
31722-010DroxidopaDroxidopa
31722-014DroxidopaDroxidopa
31722-015DroxidopaDroxidopa
50228-429Droxidopadroxidopa
50228-430Droxidopadroxidopa
50228-431Droxidopadroxidopa
59651-375DroxidopaDroxidopa
59651-376DroxidopaDroxidopa
59651-377DroxidopaDroxidopa
63304-086droxidopadroxidopa
63304-104droxidopadroxidopa
63304-112droxidopadroxidopa
67386-820Northeradroxidopa
67386-821Northeradroxidopa
67386-822Northeradroxidopa

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