Package 58988-1770-1

Brand: pyrantel pamoate

Generic: pyrantel pamoate
NDC Package

Package Facts

Identity

Package NDC 58988-1770-1
Digits Only 5898817701
Product NDC 58988-1770
Description

1 BOTTLE in 1 CARTON (58988-1770-1) / 30 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2002-09-27
Brand pyrantel pamoate
Generic pyrantel pamoate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "26fb5b42-2803-4e62-a944-b0b31ad5ba60", "openfda": {"unii": ["81BK194Z5M"], "rxcui": ["199106"], "spl_set_id": ["e68c503a-6f79-4f83-a6f3-c12a13fb06a0"], "manufacturer_name": ["ProMex LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (58988-1770-1)  / 30 mL in 1 BOTTLE", "package_ndc": "58988-1770-1", "marketing_start_date": "20020927"}], "brand_name": "Pyrantel Pamoate", "product_id": "58988-1770_26fb5b42-2803-4e62-a944-b0b31ad5ba60", "dosage_form": "SUSPENSION", "product_ndc": "58988-1770", "generic_name": "Pyrantel Pamoate", "labeler_name": "ProMex LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pyrantel Pamoate", "active_ingredients": [{"name": "PYRANTEL PAMOATE", "strength": "144 mg/mL"}], "application_number": "M024", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20020927", "listing_expiration_date": "20261231"}