Loperamide Hydrochloride

Product NDC
71335-1569
11-digit product format
713351569
Labeler code
71335
Product ID
71335-1569_7eb84e4a-afc4-40ec-9e62-2fe6ed999e2b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Loperamide Hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA073192
Marketing category
ANDA
Marketing start
1993-05-01
Marketing end
0000-00-00
Substance
LOPERAMIDE HYDROCHLORIDE
Active strength
2 mg/1
Pharmacologic classes
Opioid Agonist [EPC],Opioid Agonists [MoA]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
77TI35393CLOPERAMIDE HYDROCHLORIDE34552-83-5LOPERAMIDE HYDROCHLORIDE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1569-17133515690115 CAPSULE in 1 BOTTLE (71335-1569-1) 15 capsule1993-05-010000-00-00NoNoCurrent
71335-1569-27133515690230 CAPSULE in 1 BOTTLE (71335-1569-2) 30 capsule1993-05-010000-00-00NoNoCurrent
71335-1569-37133515690320 CAPSULE in 1 BOTTLE (71335-1569-3) 20 capsule1993-05-010000-00-00NoNoCurrent
71335-1569-47133515690412 CAPSULE in 1 BOTTLE (71335-1569-4) 12 capsule1993-05-010000-00-00NoNoCurrent
71335-1569-57133515690560 CAPSULE in 1 BOTTLE (71335-1569-5) 60 capsule1993-05-010000-00-00NoNoCurrent
71335-1569-67133515690624 CAPSULE in 1 BOTTLE (71335-1569-6) 24 capsule1993-05-010000-00-00NoNoCurrent
71335-1569-77133515690714 CAPSULE in 1 BOTTLE (71335-1569-7) 14 capsule1993-05-010000-00-00NoNoCurrent
71335-1569-8713351569089 CAPSULE in 1 BOTTLE (71335-1569-8) 9 capsule1993-05-010000-00-00NoNoCurrent