NDC 71335-1849 – Ketoconazole

Ketoconazole 200 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1849

Product details

Brand name
Ketoconazole
Generic name
Ketoconazole
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075912
Marketed since
April 10, 2020
Listing expires
December 31, 2026
Pharmacologic class
Azole Antifungal

Active ingredients

Uses, dosage, side effects and warnings for Ketoconazole →

Package NDC codes (8)

Package NDCDescriptionSince
71335-1849-110 TABLET in 1 BOTTLE (71335-1849-1)Dec 21, 2021
71335-1849-230 TABLET in 1 BOTTLE (71335-1849-2)Dec 21, 2021
71335-1849-340 TABLET in 1 BOTTLE (71335-1849-3)Dec 21, 2021
71335-1849-460 TABLET in 1 BOTTLE (71335-1849-4)Dec 21, 2021
71335-1849-58 TABLET in 1 BOTTLE (71335-1849-5)Dec 21, 2021
71335-1849-67 TABLET in 1 BOTTLE (71335-1849-6)Dec 21, 2021
71335-1849-714 TABLET in 1 BOTTLE (71335-1849-7)Dec 21, 2021
71335-1849-890 TABLET in 1 BOTTLE (71335-1849-8)Dec 21, 2021

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