MedPath
FDA Product

Droxidopa

Product approved by U.S. Food and Drug Administration (US)

Basic Information

Droxidopa

70771-1610

Regulatory Information

70771-1610

ANDA211818

C73584

August 25, 2022

USA

Droxidopa Capsules

HUMAN PRESCRIPTION DRUG LABEL

2

Company Information

918596198

Active Ingredients

DROXIDOPA

Quantity: 200 mg in 1 1

Code: J7A92W69L7

Class Code: ACTIB

FERRIC OXIDE RED

Code: 1K09F3G675

Class Code: IACT

FERRIC OXIDE YELLOW

Code: EX438O2MRT

Class Code: IACT

FERROSOFERRIC OXIDE

Code: XM0M87F357

Class Code: IACT

GELATIN

Code: 2G86QN327L

Class Code: IACT

MAGNESIUM STEARATE

Code: 70097M6I30

Class Code: IACT

MANNITOL

Code: 3OWL53L36A

Class Code: IACT

POTASSIUM HYDROXIDE

Code: WZH3C48M4T

Class Code: IACT

SHELLAC

Code: 46N107B71O

Class Code: IACT

SODIUM LAURYL SULFATE

Code: 368GB5141J

Class Code: IACT

PROPYLENE GLYCOL

Code: 6DC9Q167V3

Class Code: IACT

STARCH, CORN

Code: O8232NY3SJ

Class Code: IACT

WATER

Code: 059QF0KO0R

Class Code: IACT

TITANIUM DIOXIDE

Code: 15FIX9V2JP

Class Code: IACT

Active Moieties

DROXIDOPA

Code: J7A92W69L7

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