NDC 70710-1048 – Erythromycin

Erythromycin 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 2 recalls

Product NDC70710-1048

Product details

Brand name
Erythromycin
Generic name
Erythromycin
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA212693
Marketed since
June 30, 2023
Listing expires
December 31, 2026
Pharmacologic class
Macrolide Antimicrobial; Macrolide

Active ingredients

Uses, dosage, side effects and warnings for Erythromycin →

Package NDC codes (3)

Package NDCDescriptionSince
70710-1048-1100 TABLET, FILM COATED in 1 BOTTLE (70710-1048-1)Jun 30, 2023
70710-1048-330 TABLET, FILM COATED in 1 BOTTLE (70710-1048-3)Jun 30, 2023
70710-1048-5500 TABLET, FILM COATED in 1 BOTTLE (70710-1048-5)Jun 30, 2023

Recalls mentioning this NDC

Other Erythromycin products