Package 51079-436-20

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51079-436-20
Digits Only 5107943620
Product NDC 51079-436
Product ID 51079-436_3a3b3b4a-148f-1dc5-e063-6394a90a7bdb
Description

100 BLISTER PACK in 1 CARTON (51079-436-20) / 1 CAPSULE in 1 BLISTER PACK (51079-436-01)

Marketing

Marketing Status
Marketed Since 1998-06-12
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": "3a3b3b4a-148f-1dc5-e063-6394a90a7bdb", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000048", "1000058", "1000070", "1000076"], "spl_set_id": ["137a953b-3c48-405f-86a6-ff778cb7f5f2"], "manufacturer_name": ["Mylan Institutional Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (51079-436-20)  / 1 CAPSULE in 1 BLISTER PACK (51079-436-01)", "package_ndc": "51079-436-20", "marketing_start_date": "19980612"}], "brand_name": "Doxepin Hydrochloride", "product_id": "51079-436_3a3b3b4a-148f-1dc5-e063-6394a90a7bdb", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "51079-436", "generic_name": "doxepin hydrochloride", "labeler_name": "Mylan Institutional 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": "19980612", "listing_expiration_date": "20261231"}