Package 82868-040-14

Brand: orphenadrine citrate

Generic: orphenadrine citrate
NDC Package

Package Facts

Identity

Package NDC 82868-040-14
Digits Only 8286804014
Product NDC 82868-040
Product ID 82868-040_47f8f308-ca39-d280-e063-6394a90a49e9
Description

14 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-040-14)

Marketing

Marketing Status
Marketed Since 2024-01-30
Brand orphenadrine citrate
Generic orphenadrine citrate
Sample Package No

Linked Drug Pages (1)

ORPHENADRINE CITRATE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47f8f308-ca39-d280-e063-6394a90a49e9", "openfda": {"unii": ["X0A40N8I4S"], "rxcui": ["994521"], "spl_set_id": ["106be130-b4f8-5ca1-e063-6294a90a1590"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-040-14)", "package_ndc": "82868-040-14", "marketing_start_date": "20240130"}], "brand_name": "ORPHENADRINE CITRATE", "product_id": "82868-040_47f8f308-ca39-d280-e063-6394a90a49e9", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "82868-040", "generic_name": "ORPHENADRINE CITRATE", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ORPHENADRINE CITRATE", "active_ingredients": [{"name": "ORPHENADRINE CITRATE", "strength": "100 mg/1"}], "application_number": "ANDA040284", "marketing_category": "ANDA", "marketing_start_date": "20240130", "listing_expiration_date": "20271231"}