NDC 71335-2506 – Dicyclomine Hydrochloride

Dicyclomine Hydrochloride 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2506

Product details

Brand name
Dicyclomine Hydrochloride
Generic name
Dicyclomine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA217916
Marketed since
September 13, 2023
Listing expires
December 31, 2026
Pharmacologic class
Anticholinergic

Active ingredients

Uses, dosage, side effects and warnings for Dicyclomine Hydrochloride →

Package NDC codes (10)

Package NDCDescriptionSince
71335-2506-010 TABLET in 1 BOTTLE (71335-2506-0)Oct 7, 2024
71335-2506-130 TABLET in 1 BOTTLE (71335-2506-1)Oct 7, 2024
71335-2506-240 TABLET in 1 BOTTLE (71335-2506-2)Oct 7, 2024
71335-2506-360 TABLET in 1 BOTTLE (71335-2506-3)Oct 7, 2024
71335-2506-490 TABLET in 1 BOTTLE (71335-2506-4)Oct 7, 2024
71335-2506-520 TABLET in 1 BOTTLE (71335-2506-5)Oct 7, 2024
71335-2506-621 TABLET in 1 BOTTLE (71335-2506-6)Oct 7, 2024
71335-2506-7120 TABLET in 1 BOTTLE (71335-2506-7)Oct 7, 2024
71335-2506-8100 TABLET in 1 BOTTLE (71335-2506-8)Oct 7, 2024
71335-2506-928 TABLET in 1 BOTTLE (71335-2506-9)Oct 7, 2024

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