Package 72789-457-01

Brand: cevimeline hydrochloride

Generic: cevimeline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-457-01
Digits Only 7278945701
Product NDC 72789-457
Description

100 CAPSULE in 1 BOTTLE, PLASTIC (72789-457-01)

Marketing

Marketing Status
Marketed Since 2024-12-30
Brand cevimeline hydrochloride
Generic cevimeline hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48d8a76e-8103-9485-e063-6294a90af9ab", "openfda": {"unii": ["P81Q6V85NP"], "rxcui": ["309140"], "spl_set_id": ["2b429ea7-1c7c-47a4-803c-2546736f5c36"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE, PLASTIC (72789-457-01)", "package_ndc": "72789-457-01", "marketing_start_date": "20241230"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (72789-457-30)", "package_ndc": "72789-457-30", "marketing_start_date": "20241230"}], "brand_name": "CEVIMELINE HYDROCHLORIDE", "product_id": "72789-457_48d8a76e-8103-9485-e063-6294a90af9ab", "dosage_form": "CAPSULE", "pharm_class": ["Cholinergic Muscarinic Agonists [MoA]", "Cholinergic Receptor Agonist [EPC]"], "product_ndc": "72789-457", "generic_name": "CEVIMELINE HYDROCHLORIDE", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CEVIMELINE HYDROCHLORIDE", "active_ingredients": [{"name": "CEVIMELINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA216682", "marketing_category": "ANDA", "marketing_start_date": "20230406", "listing_expiration_date": "20271231"}