Package 27241-281-30

Brand: doxepin

Generic: doxepin
NDC Package

Package Facts

Identity

Package NDC 27241-281-30
Digits Only 2724128130
Product NDC 27241-281
Product ID 27241-281_7b7e70e8-815c-4ba4-9a9a-e7b5627ed6ea
Description

30 TABLET in 1 BOTTLE (27241-281-30)

Marketing

Marketing Status
Marketed Since 2024-07-01
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": "7b7e70e8-815c-4ba4-9a9a-e7b5627ed6ea", "openfda": {"upc": ["0327241281303", "0327241280306"], "unii": ["3U9A0FE9N5"], "rxcui": ["966787", "966793"], "spl_set_id": ["b198ade7-fe78-437e-82b4-693dfe45ab51"], "manufacturer_name": ["Ajanta Pharma USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (27241-281-30)", "package_ndc": "27241-281-30", "marketing_start_date": "20240701"}], "brand_name": "Doxepin", "product_id": "27241-281_7b7e70e8-815c-4ba4-9a9a-e7b5627ed6ea", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "27241-281", "generic_name": "Doxepin", "labeler_name": "Ajanta Pharma USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "6 mg/1"}], "application_number": "ANDA218564", "marketing_category": "ANDA", "marketing_start_date": "20240701", "listing_expiration_date": "20261231"}