NDC 71335-0311 – Diphenoxylate Hydrochloride and Atropine Sulfate

Diphenoxylate Hydrochloride 2.5 mg/1; Atropine Sulfate .025 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CV

Product NDC71335-0311

Product details

Brand name
Diphenoxylate Hydrochloride and Atropine Sulfate
Generic name
Diphenoxylate Hydrochloride and Atropine Sulfate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA086727
Marketed since
July 7, 2017
Listing expires
December 31, 2027
Pharmacologic class
Anticholinergic; Antidiarrheal; Cholinergic Muscarinic Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Diphenoxylate Hydrochloride and Atropine Sulfate →

Package NDC codes (7)

Package NDCDescriptionSince
71335-0311-120 TABLET in 1 BOTTLE (71335-0311-1)Oct 27, 2017
71335-0311-230 TABLET in 1 BOTTLE (71335-0311-2)Oct 27, 2017
71335-0311-315 TABLET in 1 BOTTLE (71335-0311-3)Oct 27, 2017
71335-0311-410 TABLET in 1 BOTTLE (71335-0311-4)Oct 27, 2017
71335-0311-540 TABLET in 1 BOTTLE (71335-0311-5)Oct 27, 2017
71335-0311-660 TABLET in 1 BOTTLE (71335-0311-6)Oct 27, 2017
71335-0311-790 TABLET in 1 BOTTLE (71335-0311-7)Oct 27, 2017

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