Package 70752-185-12

Brand: cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70752-185-12
Digits Only 7075218512
Product NDC 70752-185
Product ID 70752-185_4cf663f3-74cb-4b2c-b909-e6495d2ead78
Description

473 mL in 1 BOTTLE, PLASTIC (70752-185-12)

Marketing

Marketing Status
Marketed Since 2023-12-22
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": "4cf663f3-74cb-4b2c-b909-e6495d2ead78", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866021"], "spl_set_id": ["d3ce21de-849a-47ab-8405-968d8de6f1e9"], "manufacturer_name": ["QUAGEN PHARMACEUTICALS LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (70752-185-12)", "package_ndc": "70752-185-12", "marketing_start_date": "20231222"}], "brand_name": "CYPROHEPTADINE HYDROCHLORIDE", "product_id": "70752-185_4cf663f3-74cb-4b2c-b909-e6495d2ead78", "dosage_form": "SOLUTION", "product_ndc": "70752-185", "generic_name": "CYPROHEPTADINE HYDROCHLORIDE", "labeler_name": "QUAGEN PHARMACEUTICALS LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYPROHEPTADINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYPROHEPTADINE HYDROCHLORIDE", "strength": "2 mg/5mL"}], "application_number": "ANDA212423", "marketing_category": "ANDA", "marketing_start_date": "20231222", "listing_expiration_date": "20261231"}