Package 24208-539-20

Brand: miochol e

Generic: acetylcholine chloride
NDC Package

Package Facts

Identity

Package NDC 24208-539-20
Digits Only 2420853920
Product NDC 24208-539
Description

1 KIT in 1 BLISTER PACK (24208-539-20) * 2 mL in 1 VIAL * 2 mL in 1 AMPULE

Marketing

Marketing Status
Marketed Since 1993-09-22
Brand miochol e
Generic acetylcholine chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "19c42ee4-9f98-48da-85ea-52090070c2e2", "openfda": {"rxcui": ["876551", "876553"], "spl_set_id": ["e701ef07-9499-4b56-931f-f4eb3eedbe24"], "manufacturer_name": ["Bausch & Lomb Incorporated"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 BLISTER PACK (24208-539-20)  *  2 mL in 1 VIAL *  2 mL in 1 AMPULE", "package_ndc": "24208-539-20", "marketing_start_date": "19930922"}], "brand_name": "Miochol E", "product_id": "24208-539_19c42ee4-9f98-48da-85ea-52090070c2e2", "dosage_form": "KIT", "product_ndc": "24208-539", "generic_name": "acetylcholine chloride", "labeler_name": "Bausch & Lomb Incorporated", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Miochol E", "application_number": "NDA020213", "marketing_category": "NDA", "marketing_start_date": "19930922", "listing_expiration_date": "20261231"}