Package 43602-001-47

Brand: hydromorphone hydrochloride

Generic: hydromorphone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43602-001-47
Digits Only 4360200147
Product NDC 43602-001
Product ID 43602-001_988ded2c-ad19-48a1-a623-0f9ee982c5af
Description

473 mL in 1 BOTTLE (43602-001-47)

Marketing

Marketing Status
Marketed Since 2019-05-04
Brand hydromorphone hydrochloride
Generic hydromorphone hydrochloride
Sample Package No

Linked Drug Pages (1)

Hydromorphone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "988ded2c-ad19-48a1-a623-0f9ee982c5af", "openfda": {"upc": ["0343602279475"], "unii": ["L960UP2KRW"], "rxcui": ["897657"], "spl_set_id": ["e8fd7b0e-22b9-4f8a-8eb2-41d5031779af"], "manufacturer_name": ["Ascent Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (43602-001-47)", "package_ndc": "43602-001-47", "marketing_start_date": "20190504"}], "brand_name": "Hydromorphone Hydrochloride", "product_id": "43602-001_988ded2c-ad19-48a1-a623-0f9ee982c5af", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "43602-001", "dea_schedule": "CII", "generic_name": "Hydromorphone Hydrochloride", "labeler_name": "Ascent Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydromorphone Hydrochloride", "active_ingredients": [{"name": "HYDROMORPHONE HYDROCHLORIDE", "strength": "5 mg/5mL"}], "application_number": "ANDA210176", "marketing_category": "ANDA", "marketing_start_date": "20190504", "listing_expiration_date": "20261231"}