Package 63304-479-01

Brand: cevimeline

Generic: cevimeline
NDC Package

Package Facts

Identity

Package NDC 63304-479-01
Digits Only 6330447901
Product NDC 63304-479
Product ID 63304-479_558c3230-3788-4ef0-a5b5-3c06870317a9
Description

100 CAPSULE in 1 BOTTLE (63304-479-01)

Marketing

Marketing Status
Discontinued 2027-04-30
Brand cevimeline
Generic cevimeline
Sample Package No

Linked Drug Pages (1)

Cevimeline ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "558c3230-3788-4ef0-a5b5-3c06870317a9", "openfda": {"unii": ["P81Q6V85NP"], "rxcui": ["309140"], "spl_set_id": ["773a19e8-4c3e-4414-99a6-aea98c9790ee"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (63304-479-01)", "package_ndc": "63304-479-01", "marketing_end_date": "20270430", "marketing_start_date": "20160310"}], "brand_name": "Cevimeline", "product_id": "63304-479_558c3230-3788-4ef0-a5b5-3c06870317a9", "dosage_form": "CAPSULE", "pharm_class": ["Cholinergic Muscarinic Agonists [MoA]", "Cholinergic Receptor Agonist [EPC]"], "product_ndc": "63304-479", "generic_name": "Cevimeline", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cevimeline", "active_ingredients": [{"name": "CEVIMELINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "NDA020989", "marketing_category": "NDA", "marketing_end_date": "20270430", "marketing_start_date": "20160310"}