Package 58657-697-16

Brand: cyproheptadine hydrochloride solution

Generic: cyproheptadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 58657-697-16
Digits Only 5865769716
Product NDC 58657-697
Description

473 mL in 1 BOTTLE, GLASS (58657-697-16)

Marketing

Marketing Status
Marketed Since 2024-06-15
Brand cyproheptadine hydrochloride solution
Generic cyproheptadine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41b48ab2-962e-790a-e063-6394a90a6106", "openfda": {"upc": ["0358657697167"], "unii": ["2YHB6175DO"], "rxcui": ["866021"], "spl_set_id": ["1acfd050-6c07-a269-e063-6394a90a77e8"], "manufacturer_name": ["Method Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, GLASS (58657-697-16)", "package_ndc": "58657-697-16", "marketing_start_date": "20240615"}], "brand_name": "cyproheptadine hydrochloride solution", "product_id": "58657-697_41b48ab2-962e-790a-e063-6394a90a6106", "dosage_form": "SOLUTION", "product_ndc": "58657-697", "generic_name": "CYPROHEPTADINE HYDROCHLORIDE", "labeler_name": "Method Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "cyproheptadine hydrochloride solution", "active_ingredients": [{"name": "CYPROHEPTADINE", "strength": "2 mg/5mL"}], "application_number": "ANDA209108", "marketing_category": "ANDA", "marketing_start_date": "20240615", "listing_expiration_date": "20261231"}