Package 68788-7842-1

Brand: loperamide hydrochloride

Generic: loperamide hcl
NDC Package

Package Facts

Identity

Package NDC 68788-7842-1
Digits Only 6878878421
Product NDC 68788-7842
Description

120 mL in 1 BOTTLE (68788-7842-1)

Marketing

Marketing Status
Marketed Since 2021-01-19
Brand loperamide hydrochloride
Generic loperamide hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5f21733b-73e8-42b7-91af-059e5667ef91", "openfda": {"unii": ["77TI35393C"], "rxcui": ["1250685"], "spl_set_id": ["0b1f8d41-51b3-4362-8de7-46bca5caff12"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "120 mL in 1 BOTTLE (68788-7842-1)", "package_ndc": "68788-7842-1", "marketing_start_date": "20210119"}], "brand_name": "loperamide hydrochloride", "product_id": "68788-7842_5f21733b-73e8-42b7-91af-059e5667ef91", "dosage_form": "SOLUTION", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "68788-7842", "generic_name": "loperamide HCl", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "loperamide hydrochloride", "active_ingredients": [{"name": "LOPERAMIDE HYDROCHLORIDE", "strength": "1 mg/7.5mL"}], "application_number": "ANDA091292", "marketing_category": "ANDA", "marketing_start_date": "20210119", "listing_expiration_date": "20261231"}