NDC 71335-2226 – Dicyclomine hydrochloride

Dicyclomine Hydrochloride 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2226

Product details

Brand name
Dicyclomine hydrochloride
Generic name
Dicyclomine hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA216736
Marketed since
December 14, 2022
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
71335-2226-010 TABLET in 1 BOTTLE (71335-2226-0)Aug 23, 2023
71335-2226-130 TABLET in 1 BOTTLE (71335-2226-1)Aug 23, 2023
71335-2226-240 TABLET in 1 BOTTLE (71335-2226-2)Aug 23, 2023
71335-2226-360 TABLET in 1 BOTTLE (71335-2226-3)Aug 23, 2023
71335-2226-490 TABLET in 1 BOTTLE (71335-2226-4)Aug 23, 2023
71335-2226-520 TABLET in 1 BOTTLE (71335-2226-5)Aug 23, 2023
71335-2226-621 TABLET in 1 BOTTLE (71335-2226-6)Aug 23, 2023
71335-2226-7120 TABLET in 1 BOTTLE (71335-2226-7)Aug 23, 2023
71335-2226-8100 TABLET in 1 BOTTLE (71335-2226-8)Aug 23, 2023
71335-2226-928 TABLET in 1 BOTTLE (71335-2226-9)Aug 23, 2023

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