NDC 71335-1921 – Loperamide Hydrochloride

Loperamide Hydrochloride 2 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-1921

Product details

Brand name
Loperamide Hydrochloride
Generic name
Loperamide hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA072741
Marketed since
September 18, 1991
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (10)

Package NDCDescriptionSince
71335-1921-050 CAPSULE in 1 BOTTLE, PLASTIC (71335-1921-0)May 3, 2022
71335-1921-115 CAPSULE in 1 BOTTLE, PLASTIC (71335-1921-1)Jul 30, 2021
71335-1921-230 CAPSULE in 1 BOTTLE, PLASTIC (71335-1921-2)Aug 30, 2021
71335-1921-320 CAPSULE in 1 BOTTLE, PLASTIC (71335-1921-3)Aug 18, 2021
71335-1921-412 CAPSULE in 1 BOTTLE, PLASTIC (71335-1921-4)Aug 20, 2021
71335-1921-560 CAPSULE in 1 BOTTLE, PLASTIC (71335-1921-5)May 3, 2022
71335-1921-624 CAPSULE in 1 BOTTLE, PLASTIC (71335-1921-6)Jul 30, 2021
71335-1921-714 CAPSULE in 1 BOTTLE, PLASTIC (71335-1921-7)May 3, 2022
71335-1921-89 CAPSULE in 1 BOTTLE, PLASTIC (71335-1921-8)Jul 26, 2021
71335-1921-95 CAPSULE in 1 BOTTLE, PLASTIC (71335-1921-9)Feb 23, 2022

Other Loperamide Hydrochloride products