Package 0054-3545-63

Brand: meperidine hydrochloride

Generic: meperidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0054-3545-63
Digits Only 0054354563
Product NDC 0054-3545
Description

500 mL in 1 BOTTLE (0054-3545-63)

Marketing

Marketing Status
Marketed Since 1985-01-30
Brand meperidine hydrochloride
Generic meperidine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "677fb454-d83d-4c3c-b095-a58a1c4781b9", "openfda": {"upc": ["0300543545632"], "unii": ["N8E7F7Q170"], "rxcui": ["861455", "861467", "861479"], "spl_set_id": ["15bc51a8-1e24-4d33-9a2f-05a41c29acf0"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BOTTLE (0054-3545-63)", "package_ndc": "0054-3545-63", "marketing_start_date": "19850130"}], "brand_name": "Meperidine Hydrochloride", "product_id": "0054-3545_677fb454-d83d-4c3c-b095-a58a1c4781b9", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0054-3545", "dea_schedule": "CII", "generic_name": "Meperidine Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Meperidine Hydrochloride", "active_ingredients": [{"name": "MEPERIDINE HYDROCHLORIDE", "strength": "50 mg/5mL"}], "application_number": "ANDA088744", "marketing_category": "ANDA", "marketing_start_date": "19850130", "listing_expiration_date": "20271231"}