Package 0641-6052-25
Brand: meperidine hydrochloride
Generic: meperidine hydrochloridePackage Facts
Identity
Package NDC
0641-6052-25
Digits Only
0641605225
Product NDC
0641-6052
Description
25 VIAL in 1 CARTON (0641-6052-25) / 1 mL in 1 VIAL (0641-6052-01)
Marketing
Marketing Status
Brand
meperidine hydrochloride
Generic
meperidine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "9566d54d-7343-4695-94ff-8b5f2d384c81", "openfda": {"unii": ["N8E7F7Q170"], "rxcui": ["861476", "1665685", "1665697"], "spl_set_id": ["e0e998da-f056-4fce-be8e-ed60cf3b461b"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (0641-6052-25) / 1 mL in 1 VIAL (0641-6052-01)", "package_ndc": "0641-6052-25", "marketing_start_date": "19750122"}], "brand_name": "MEPERIDINE HYDROCHLORIDE", "product_id": "0641-6052_9566d54d-7343-4695-94ff-8b5f2d384c81", "dosage_form": "INJECTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0641-6052", "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": "25 mg/mL"}], "application_number": "ANDA080445", "marketing_category": "ANDA", "marketing_start_date": "19750122", "listing_expiration_date": "20261231"}