Package 0703-0113-03
Brand: hydromorphone hydrochloride
Generic: hydromorphone hydrochloridePackage Facts
Identity
Package NDC
0703-0113-03
Digits Only
0703011303
Product NDC
0703-0113
Description
10 VIAL in 1 CARTON (0703-0113-03) / 5 mL in 1 VIAL (0703-0113-01)
Marketing
Marketing Status
Brand
hydromorphone hydrochloride
Generic
hydromorphone hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "c32108cc-7b73-4921-9f9e-54b3d60c1c6e", "openfda": {"upc": ["0307030110038"], "unii": ["L960UP2KRW"], "rxcui": ["1724338", "1724340", "1724341"], "spl_set_id": ["f0b78db9-a38c-41bb-8233-5e93f7f18c5c"], "manufacturer_name": ["Teva Parenteral Medicines, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (0703-0113-03) / 5 mL in 1 VIAL (0703-0113-01)", "package_ndc": "0703-0113-03", "marketing_start_date": "20110118"}], "brand_name": "Hydromorphone Hydrochloride", "product_id": "0703-0113_c32108cc-7b73-4921-9f9e-54b3d60c1c6e", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0703-0113", "dea_schedule": "CII", "generic_name": "HYDROMORPHONE HYDROCHLORIDE", "labeler_name": "Teva Parenteral Medicines, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydromorphone Hydrochloride", "active_ingredients": [{"name": "HYDROMORPHONE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA078591", "marketing_category": "ANDA", "marketing_start_date": "20110118", "listing_expiration_date": "20261231"}