Package 10135-758-30

Brand: doxepin

Generic: doxepin
NDC Package

Package Facts

Identity

Package NDC 10135-758-30
Digits Only 1013575830
Product NDC 10135-758
Product ID 10135-758_43029ddd-8941-add8-e063-6394a90a1e4d
Description

30 TABLET, FILM COATED in 1 BOTTLE (10135-758-30)

Marketing

Marketing Status
Marketed Since 2023-10-01
Brand doxepin
Generic doxepin
Sample Package No

Linked Drug Pages (1)

Doxepin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "43029ddd-8941-add8-e063-6394a90a1e4d", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["966787", "966793"], "spl_set_id": ["06e79a65-1455-804e-e063-6394a90a2f3d"], "manufacturer_name": ["Marlex Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (10135-758-30)", "package_ndc": "10135-758-30", "marketing_start_date": "20231001"}], "brand_name": "Doxepin", "product_id": "10135-758_43029ddd-8941-add8-e063-6394a90a1e4d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "10135-758", "generic_name": "Doxepin", "labeler_name": "Marlex Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "3 mg/1"}], "application_number": "ANDA202337", "marketing_category": "ANDA", "marketing_start_date": "20231001", "listing_expiration_date": "20261231"}