Package 43063-740-01

Brand: methscopolamine bromide

Generic: methscopolamine bromide
NDC Package

Package Facts

Identity

Package NDC 43063-740-01
Digits Only 4306374001
Product NDC 43063-740
Product ID 43063-740_47a6aa83-d825-90c6-e063-6394a90acd31
Description

100 TABLET in 1 BOTTLE, PLASTIC (43063-740-01)

Marketing

Marketing Status
Marketed Since 2017-02-01
Brand methscopolamine bromide
Generic methscopolamine bromide
Sample Package No

Linked Drug Pages (1)

METHSCOPOLAMINE BROMIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47a6aa83-d825-90c6-e063-6394a90acd31", "openfda": {"upc": ["0343063740019"], "unii": ["RTN51LK7WL"], "rxcui": ["314088"], "spl_set_id": ["26cd56db-4727-40d1-8f08-3ee899052c77"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (43063-740-01)", "package_ndc": "43063-740-01", "marketing_start_date": "20170201"}], "brand_name": "METHSCOPOLAMINE BROMIDE", "product_id": "43063-740_47a6aa83-d825-90c6-e063-6394a90acd31", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "43063-740", "generic_name": "methscopolamine bromide", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHSCOPOLAMINE BROMIDE", "active_ingredients": [{"name": "METHSCOPOLAMINE BROMIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA200602", "marketing_category": "ANDA", "marketing_start_date": "20131001", "listing_expiration_date": "20271231"}