Package 16477-202-12

Brand: hemmorex-hc

Generic: hydrocortisone acetate
NDC Package

Package Facts

Identity

Package NDC 16477-202-12
Digits Only 1647720212
Product NDC 16477-202
Description

12 SUPPOSITORY in 1 BOX (16477-202-12)

Marketing

Marketing Status
Marketed Since 2021-08-02
Brand hemmorex-hc
Generic hydrocortisone acetate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["RECTAL"], "spl_id": "47d761e2-d5ae-52a0-e063-6394a90a94e1", "openfda": {"unii": ["3X7931PO74"], "rxcui": ["1291085", "1674200"], "spl_set_id": ["d625764a-6171-4802-9bc0-95e5785b8b7d"], "manufacturer_name": ["Laser Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 SUPPOSITORY in 1 BOX (16477-202-12)", "package_ndc": "16477-202-12", "marketing_start_date": "20210802"}], "brand_name": "Hemmorex-HC", "product_id": "16477-202_47d761e2-d5ae-52a0-e063-6394a90a94e1", "dosage_form": "SUPPOSITORY", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "16477-202", "generic_name": "hydrocortisone acetate", "labeler_name": "Laser Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hemmorex-HC", "active_ingredients": [{"name": "HYDROCORTISONE ACETATE", "strength": "30 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20131112", "listing_expiration_date": "20271231"}