Package 64980-504-48

Brand: cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 64980-504-48
Digits Only 6498050448
Product NDC 64980-504
Product ID 64980-504_9b4845c1-9b59-4809-9247-50565fc4b6fb
Description

473 mL in 1 BOTTLE (64980-504-48)

Marketing

Marketing Status
Marketed Since 2006-07-10
Brand cyproheptadine hydrochloride
Generic cyproheptadine hydrochloride
Sample Package No

Linked Drug Pages (1)

Cyproheptadine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9b4845c1-9b59-4809-9247-50565fc4b6fb", "openfda": {"upc": ["0364980504485"], "unii": ["NJ82J0F8QC"], "rxcui": ["866021"], "spl_set_id": ["e2bf4d46-6585-41d9-868c-98603b165d5b"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (64980-504-48)", "package_ndc": "64980-504-48", "marketing_start_date": "20060710"}], "brand_name": "Cyproheptadine Hydrochloride", "product_id": "64980-504_9b4845c1-9b59-4809-9247-50565fc4b6fb", "dosage_form": "SYRUP", "product_ndc": "64980-504", "generic_name": "Cyproheptadine Hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyproheptadine Hydrochloride", "active_ingredients": [{"name": "CYPROHEPTADINE HYDROCHLORIDE", "strength": "2 mg/5mL"}], "application_number": "ANDA040668", "marketing_category": "ANDA", "marketing_start_date": "20060710", "listing_expiration_date": "20261231"}