NDC 0093-1087 – Cefaclor

Cefaclor 500 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC0093-1087

Product details

Brand name
Cefaclor
Generic name
Cefaclor
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA065058
Marketed since
September 26, 2002
Listing expires
December 31, 2026
Pharmacologic class
Cephalosporin Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Cefaclor →

Package NDC codes (1)

Package NDCDescriptionSince
0093-1087-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-1087-01)Sep 26, 2002

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