Hydroxychloroquine Sulfate 68071-2332-01

Package NDC

68071-2332-01

Manufacturer: Nucare Pharmaceuticals,inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: October 1, 2019
Listing Expires: December 31, 2026
Application: ANDA040657

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Active Ingredients

Ingredient	Strength
Hydroxychloroquine Sulfate	200 mg/1

Drug Class

Antimalarial [EPC]Antirheumatic Agent [EPC]

Selected Package

68071-2332-01Selected

100 TABLET, FILM COATED in 1 BOTTLE (68071-2332-1)