Package 0378-3125-01

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0378-3125-01
Digits Only 0378312501
Product NDC 0378-3125
Product ID 0378-3125_335104fb-31eb-4460-b3ab-19869176b320
Description

100 CAPSULE in 1 BOTTLE, PLASTIC (0378-3125-01)

Marketing

Marketing Status
Marketed Since 1986-05-13
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": "335104fb-31eb-4460-b3ab-19869176b320", "openfda": {"upc": ["0303785375012", "0303786410019", "0303784250013", "0303781049016", "0303783125015"], "unii": ["3U9A0FE9N5"], "rxcui": ["1000048", "1000058", "1000070", "1000076", "1000097"], "spl_set_id": ["1533343b-f1ed-4c3a-bb36-23a748452b05"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE, PLASTIC (0378-3125-01)", "package_ndc": "0378-3125-01", "marketing_start_date": "19860513"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE, PLASTIC (0378-3125-10)", "package_ndc": "0378-3125-10", "marketing_start_date": "19860513"}], "brand_name": "Doxepin Hydrochloride", "product_id": "0378-3125_335104fb-31eb-4460-b3ab-19869176b320", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "0378-3125", "generic_name": "doxepin hydrochloride", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA070791", "marketing_category": "ANDA", "marketing_start_date": "19860513", "listing_expiration_date": "20261231"}