Package 72789-072-30

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-072-30
Digits Only 7278907230
Product NDC 72789-072
Product ID 72789-072_47a923cf-2731-8fc9-e063-6294a90afa38
Description

30 CAPSULE in 1 BOTTLE, PLASTIC (72789-072-30)

Marketing

Marketing Status
Marketed Since 2020-04-01
Brand doxepin hydrochloride
Generic doxepin hydrochloride
Sample Package No

Linked Drug Pages (1)

Doxepin Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47a923cf-2731-8fc9-e063-6294a90afa38", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000048"], "spl_set_id": ["d2a91b99-513d-4894-ad6d-02d2028a2290"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (72789-072-30)", "package_ndc": "72789-072-30", "marketing_start_date": "20200401"}], "brand_name": "Doxepin Hydrochloride", "product_id": "72789-072_47a923cf-2731-8fc9-e063-6294a90afa38", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72789-072", "generic_name": "doxepin hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA070791", "marketing_category": "ANDA", "marketing_start_date": "19860513", "listing_expiration_date": "20271231"}