NDC 71335-2010 – Bisacodyl

Bisacodyl 5 mg/1 · Tablet, Delayed Release · Oral

Human Otc Drug

Product NDC71335-2010

Product details

Brand name
Bisacodyl
Generic name
Bisacodyl
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
OTC MONOGRAPH DRUG · 505G(a)(3)
Marketed since
December 1, 2018
Listing expires
December 31, 2026
Pharmacologic class
Stimulant Laxative

Active ingredients

Uses, dosage, side effects and warnings for Bisacodyl →

Package NDC codes (10)

Package NDCDescriptionSince
71335-2010-025 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2010-0)Apr 3, 2024
71335-2010-130 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2010-1)Mar 3, 2022
71335-2010-22 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2010-2)Apr 3, 2024
71335-2010-33 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2010-3)Apr 3, 2024
71335-2010-44 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2010-4)Jan 3, 2022
71335-2010-510 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2010-5)Jan 18, 2022
71335-2010-690 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2010-6)Apr 3, 2024
71335-2010-78 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2010-7)Jan 12, 2022
71335-2010-8100 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2010-8)Apr 3, 2024
71335-2010-920 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2010-9)Apr 3, 2024

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