loperamide hydrochloride and simethicone
Generic: loperamide hydrochloride and simethicone
Labeler: aurohealth llcDrug Facts
Product Profile
Brand Name
loperamide hydrochloride and simethicone
Generic Name
loperamide hydrochloride and simethicone
Labeler
aurohealth llc
Dosage Form
TABLET
Routes
Active Ingredients
dimethicone 125 mg/1, loperamide hydrochloride 2 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
58602-815
Product ID
58602-815_f2788da1-1ef1-4db9-8271-e786cc2ddd9e
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA211059
Listing Expiration
2026-12-31
Marketing Start
2020-12-14
Pharmacologic Class
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
58602815
Hyphenated Format
58602-815
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 125 mg/1
- 2 mg/1
Packaging
- 1 BLISTER PACK in 1 CARTON (58602-815-74) / 6 TABLET in 1 BLISTER PACK
- 2 BLISTER PACK in 1 CARTON (58602-815-75) / 6 TABLET in 1 BLISTER PACK
- 4 BLISTER PACK in 1 CARTON (58602-815-76) / 6 TABLET in 1 BLISTER PACK
- 3 BLISTER PACK in 1 CARTON (58602-815-80) / 6 TABLET in 1 BLISTER PACK
Packages (4)
58602-815-74
1 BLISTER PACK in 1 CARTON (58602-815-74) / 6 TABLET in 1 BLISTER PACK
58602-815-75
2 BLISTER PACK in 1 CARTON (58602-815-75) / 6 TABLET in 1 BLISTER PACK
58602-815-76
4 BLISTER PACK in 1 CARTON (58602-815-76) / 6 TABLET in 1 BLISTER PACK
58602-815-80
3 BLISTER PACK in 1 CARTON (58602-815-80) / 6 TABLET in 1 BLISTER PACK
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f2788da1-1ef1-4db9-8271-e786cc2ddd9e", "openfda": {"nui": ["N0000010282"], "unii": ["92RU3N3Y1O", "77TI35393C"], "rxcui": ["978001"], "spl_set_id": ["9dd3a6d6-9fff-45b3-8e76-57bf5ee2e07f"], "pharm_class_pe": ["Skin Barrier Activity [PE]"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (58602-815-74) / 6 TABLET in 1 BLISTER PACK", "package_ndc": "58602-815-74", "marketing_start_date": "20201214"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (58602-815-75) / 6 TABLET in 1 BLISTER PACK", "package_ndc": "58602-815-75", "marketing_start_date": "20201214"}, {"sample": false, "description": "4 BLISTER PACK in 1 CARTON (58602-815-76) / 6 TABLET in 1 BLISTER PACK", "package_ndc": "58602-815-76", "marketing_start_date": "20201214"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (58602-815-80) / 6 TABLET in 1 BLISTER PACK", "package_ndc": "58602-815-80", "marketing_start_date": "20201214"}], "brand_name": "Loperamide Hydrochloride and Simethicone", "product_id": "58602-815_f2788da1-1ef1-4db9-8271-e786cc2ddd9e", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]", "Skin Barrier Activity [PE]"], "product_ndc": "58602-815", "generic_name": "Loperamide Hydrochloride and Simethicone", "labeler_name": "Aurohealth LLC", "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": "20201214", "listing_expiration_date": "20261231"}