Package 70752-107-10

Brand: cyproheptadine hydrochloride

Generic: cyproheptadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70752-107-10
Digits Only 7075210710
Product NDC 70752-107
Description

100 TABLET in 1 BOTTLE, PLASTIC (70752-107-10)

Marketing

Marketing Status
Marketed Since 2021-02-24
Brand cyproheptadine hydrochloride
Generic cyproheptadine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c83adc2f-bfdf-4fa5-b95b-2a190a7fd78f", "openfda": {"unii": ["NJ82J0F8QC"], "rxcui": ["866144"], "spl_set_id": ["98e71865-83dd-4e29-8308-c56e36731d96"], "manufacturer_name": ["QUAGEN PHARMACEUTICALS LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (70752-107-10)", "package_ndc": "70752-107-10", "marketing_start_date": "20210224"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (70752-107-11)", "package_ndc": "70752-107-11", "marketing_start_date": "20210224"}], "brand_name": "CYPROHEPTADINE HYDROCHLORIDE", "product_id": "70752-107_c83adc2f-bfdf-4fa5-b95b-2a190a7fd78f", "dosage_form": "TABLET", "product_ndc": "70752-107", "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": "4 mg/1"}], "application_number": "ANDA212491", "marketing_category": "ANDA", "marketing_start_date": "20210224", "listing_expiration_date": "20261231"}