Package 0713-0937-01

Brand: cevimeline hydrochloride

Generic: cevimeline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0713-0937-01
Digits Only 0713093701
Product NDC 0713-0937
Description

100 CAPSULE in 1 BOTTLE, PLASTIC (0713-0937-01)

Marketing

Marketing Status
Marketed Since 2023-01-03
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": "f183f958-57f5-ea10-e053-2995a90a5ead", "openfda": {"upc": ["0307130937016"], "unii": ["P81Q6V85NP"], "rxcui": ["309140"], "spl_set_id": ["efc2bb24-4dda-4781-bef5-fcd9abf082dd"], "manufacturer_name": ["Cosette Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE, PLASTIC (0713-0937-01)", "package_ndc": "0713-0937-01", "marketing_start_date": "20230103"}], "brand_name": "cevimeline hydrochloride", "product_id": "0713-0937_f183f958-57f5-ea10-e053-2995a90a5ead", "dosage_form": "CAPSULE", "pharm_class": ["Cholinergic Muscarinic Agonists [MoA]", "Cholinergic Receptor Agonist [EPC]"], "product_ndc": "0713-0937", "generic_name": "cevimeline hydrochloride", "labeler_name": "Cosette Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "cevimeline hydrochloride", "active_ingredients": [{"name": "CEVIMELINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "NDA020989", "marketing_category": "NDA", "marketing_start_date": "20230103", "listing_expiration_date": "20261231"}