NDC 71335-2111 – Loperamide Hydrochloride

Loperamide Hydrochloride 2 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-2111

Product details

Brand name
Loperamide Hydrochloride
Generic name
Loperamide Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA215001
Marketed since
September 25, 2020
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (10)

Package NDCDescriptionSince
71335-2111-050 CAPSULE in 1 BOTTLE (71335-2111-0)Jun 20, 2022
71335-2111-115 CAPSULE in 1 BOTTLE (71335-2111-1)Jun 20, 2022
71335-2111-230 CAPSULE in 1 BOTTLE (71335-2111-2)Jun 20, 2022
71335-2111-320 CAPSULE in 1 BOTTLE (71335-2111-3)Jun 20, 2022
71335-2111-412 CAPSULE in 1 BOTTLE (71335-2111-4)Jun 20, 2022
71335-2111-560 CAPSULE in 1 BOTTLE (71335-2111-5)Jun 20, 2022
71335-2111-624 CAPSULE in 1 BOTTLE (71335-2111-6)Jun 20, 2022
71335-2111-714 CAPSULE in 1 BOTTLE (71335-2111-7)Jun 20, 2022
71335-2111-89 CAPSULE in 1 BOTTLE (71335-2111-8)Jun 20, 2022
71335-2111-95 CAPSULE in 1 BOTTLE (71335-2111-9)Jun 20, 2022

Other Loperamide Hydrochloride products