NDC 62135-842 – sulfADIAZINE

Sulfadiazine 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC62135-842

Product details

Brand name
sulfADIAZINE
Generic name
sulfADIAZINE
Labeler
Chartwell RX, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA080084
Marketed since
September 23, 2024
Listing expires
December 31, 2026
Pharmacologic class
Sulfonamide Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for sulfADIAZINE →

Package NDC codes (1)

Package NDCDescriptionSince
62135-842-6060 TABLET in 1 BOTTLE (62135-842-60)Sep 23, 2024

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