Loperamide Hydrochloride and Simethicone

Product NDC
58602-868
11-digit product format
586020868
Labeler code
58602
Product ID
58602-868_cbeb5700-40fc-4140-862f-661f864ecd25
Type
HUMAN OTC DRUG
Nonproprietary name
Loperamide Hydrochloride and Simethicone
Dosage form
TABLET
Route
ORAL
Labeler
Aurohealth LLC
Application
ANDA211059
Marketing category
ANDA
Marketing start
2021-02-24
Substance
DIMETHICONE; LOPERAMIDE HYDROCHLORIDE
Active strength
125; 2 mg/1; mg/1
Pharmacologic classes
Opioid Agonist [EPC], Opioid Agonists [MoA], Skin Barrier Activity [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Loperamide Hydrochloride and Simethicone
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
DIMETHICONE125 mg/1
LOPERAMIDE HYDROCHLORIDE2 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii92RU3N3Y1O, 77TI35393C
Rxcui978001

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
10f838ef-a72b-645d-80f8-e2255205c3b1Product name620240805

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58602-868-76Loperamide Hydrochloride and Simethicone4 in 1 CARTONTABLET45
58602-868-76Loperamide Hydrochloride and Simethicone6 in 1 BLISTER PACKTABLET65

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58602-868LOPERAMIDE HYDROCHLORIDE AND SIMETHICONE TABLET [AUROHEALTH LLC]5Current NDC, Legacy NDC, 2 package rows20250112_d388f536-704a-4d6e-ab27-c1a96e939413.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
58602-868-76586020868764 BLISTER PACK in 1 CARTON (58602-868-76) / 6 TABLET in 1 BLISTER PACK4 blister pack2021-02-240000-00-00NoNoCurrent