Package 60687-229-01

Brand: loperamide hydrochloride

Generic: loperamide hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-229-01
Digits Only 6068722901
Product NDC 60687-229
Product ID 60687-229_437e8cc1-d818-dac5-e063-6294a90a1752
Description

100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-229-01) / 1 CAPSULE in 1 BLISTER PACK (60687-229-11)

Marketing

Marketing Status
Marketed Since 2017-01-03
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": "437e8cc1-d818-dac5-e063-6294a90a1752", "openfda": {"unii": ["77TI35393C"], "rxcui": ["978006"], "spl_set_id": ["42989f90-8ff5-44d1-a462-28c18ce02738"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-229-01)  / 1 CAPSULE in 1 BLISTER PACK (60687-229-11)", "package_ndc": "60687-229-01", "marketing_start_date": "20170103"}], "brand_name": "Loperamide Hydrochloride", "product_id": "60687-229_437e8cc1-d818-dac5-e063-6294a90a1752", "dosage_form": "CAPSULE", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "60687-229", "generic_name": "Loperamide Hydrochloride", "labeler_name": "American Health Packaging", "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": "20170103", "listing_expiration_date": "20261231"}