Package 43063-020-12

Brand: loperamide hydrochloride

Generic: loperamide hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43063-020-12
Digits Only 4306302012
Product NDC 43063-020
Product ID 43063-020_413648bd-6784-dfcf-e063-6294a90a7d88
Description

12 CAPSULE in 1 BOTTLE, PLASTIC (43063-020-12)

Marketing

Marketing Status
Marketed Since 2008-10-28
Brand loperamide hydrochloride
Generic loperamide hydrochloride
Sample Package No

Linked Drug Pages (1)

Loperamide Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "413648bd-6784-dfcf-e063-6294a90a7d88", "openfda": {"unii": ["77TI35393C"], "rxcui": ["978006"], "spl_set_id": ["580e6cd4-3f05-4996-9dc3-c50d757ae210"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "12 CAPSULE in 1 BOTTLE, PLASTIC (43063-020-12)", "package_ndc": "43063-020-12", "marketing_start_date": "20081028"}], "brand_name": "Loperamide Hydrochloride", "product_id": "43063-020_413648bd-6784-dfcf-e063-6294a90a7d88", "dosage_form": "CAPSULE", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "43063-020", "generic_name": "Loperamide Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Loperamide Hydrochloride", "active_ingredients": [{"name": "LOPERAMIDE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA073192", "marketing_category": "ANDA", "marketing_start_date": "19930501", "listing_expiration_date": "20261231"}