Package 59088-391-00

Brand: dermacinrx clorhexacin

Generic: mupirocin ointment
NDC Package

Package Facts

Identity

Package NDC 59088-391-00
Digits Only 5908839100
Product NDC 59088-391
Description

1 KIT in 1 CARTON (59088-391-00) * 237 mL in 1 BOTTLE, PLASTIC (0116-1061-08) * 118 mL in 1 TUBE (59088-333-08) * 1 TUBE in 1 CARTON (45802-112-22) / 22 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2016-06-02
Brand dermacinrx clorhexacin
Generic mupirocin ointment
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "292fb349-6c9f-d1dd-e063-6394a90a5ed9", "openfda": {"rxcui": ["106346", "211365", "259090"], "spl_set_id": ["3c8cb9a6-58e5-4e8d-bfdc-1432a1bde6f9"], "manufacturer_name": ["PureTek Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (59088-391-00)  *  237 mL in 1 BOTTLE, PLASTIC (0116-1061-08)  *  118 mL in 1 TUBE (59088-333-08)  *  1 TUBE in 1 CARTON (45802-112-22)  / 22 g in 1 TUBE", "package_ndc": "59088-391-00", "marketing_start_date": "20160602"}], "brand_name": "DermacinRx Clorhexacin", "product_id": "59088-391_292fb349-6c9f-d1dd-e063-6394a90a5ed9", "dosage_form": "KIT", "product_ndc": "59088-391", "generic_name": "Mupirocin Ointment", "labeler_name": "PureTek Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DermacinRx Clorhexacin", "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20160602", "listing_expiration_date": "20261231"}