loperamide hydrochloride and simethicone

Generic: loperamide hydrochloride and simethicone

Labeler: walmart inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name loperamide hydrochloride and simethicone
Generic Name loperamide hydrochloride and simethicone
Labeler walmart inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

dimethicone 125 mg/1, loperamide hydrochloride 2 mg/1

Manufacturer
WALMART INC.

Identifiers & Regulatory

Product NDC 79903-223
Product ID 79903-223_d5cdb88f-1858-4e14-a988-2db6865255c5
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA211059
Listing Expiration 2026-12-31
Marketing Start 2024-02-17

Pharmacologic Class

Physiologic Effect
skin barrier activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 79903223
Hyphenated Format 79903-223

Supplemental Identifiers

RxCUI
978001
UNII
92RU3N3Y1O 77TI35393C
NUI
N0000010282

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name loperamide hydrochloride and simethicone (source: ndc)
Generic Name loperamide hydrochloride and simethicone (source: ndc)
Application Number ANDA211059 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 125 mg/1
  • 2 mg/1
source: ndc
Packaging
  • 2 BLISTER PACK in 1 CARTON (79903-223-12) / 6 TABLET in 1 BLISTER PACK
  • 4 BLISTER PACK in 1 CARTON (79903-223-24) / 6 TABLET in 1 BLISTER PACK
source: ndc

Packages (2)

Ingredients (2)

dimethicone (125 mg/1) loperamide hydrochloride (2 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d5cdb88f-1858-4e14-a988-2db6865255c5", "openfda": {"nui": ["N0000010282"], "unii": ["92RU3N3Y1O", "77TI35393C"], "rxcui": ["978001"], "spl_set_id": ["12940c3b-dc58-31fb-e063-6294a90ae880"], "pharm_class_pe": ["Skin Barrier Activity [PE]"], "manufacturer_name": ["WALMART INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (79903-223-12)  / 6 TABLET in 1 BLISTER PACK", "package_ndc": "79903-223-12", "marketing_start_date": "20240217"}, {"sample": false, "description": "4 BLISTER PACK in 1 CARTON (79903-223-24)  / 6 TABLET in 1 BLISTER PACK", "package_ndc": "79903-223-24", "marketing_start_date": "20240217"}], "brand_name": "Loperamide Hydrochloride and Simethicone", "product_id": "79903-223_d5cdb88f-1858-4e14-a988-2db6865255c5", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]", "Skin Barrier Activity [PE]"], "product_ndc": "79903-223", "generic_name": "Loperamide Hydrochloride and Simethicone", "labeler_name": "WALMART INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loperamide Hydrochloride and Simethicone", "active_ingredients": [{"name": "DIMETHICONE", "strength": "125 mg/1"}, {"name": "LOPERAMIDE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA211059", "marketing_category": "ANDA", "marketing_start_date": "20240217", "listing_expiration_date": "20261231"}