doxepin hydrochloride

Generic: doxepin hydrochloride

Labeler: epic pharma, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxepin hydrochloride
Generic Name doxepin hydrochloride
Labeler epic pharma, llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

doxepin hydrochloride 100 mg/1

Manufacturer
Epic Pharma, LLC

Identifiers & Regulatory

Product NDC 42806-533
Product ID 42806-533_a5adf083-8dd9-4482-a3f1-589ade22b653
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210675
Listing Expiration 2026-12-31
Marketing Start 2017-06-06

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42806533
Hyphenated Format 42806-533

Supplemental Identifiers

RxCUI
1000048 1000058 1000070 1000076 1000097
UNII
3U9A0FE9N5

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name doxepin hydrochloride (source: ndc)
Generic Name doxepin hydrochloride (source: ndc)
Application Number ANDA210675 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (42806-533-01)
  • 1000 CAPSULE in 1 BOTTLE (42806-533-10)
source: ndc

Packages (2)

42806-533-01 100 CAPSULE in 1 BOTTLE (42806-533-01) 42806-533-10 1000 CAPSULE in 1 BOTTLE (42806-533-10)

Ingredients (1)

doxepin hydrochloride (100 mg/1)

Linked Drug Pages (1)

Doxepin Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a5adf083-8dd9-4482-a3f1-589ade22b653", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000048", "1000058", "1000070", "1000076", "1000097"], "spl_set_id": ["5f0f6fee-2497-4915-b58b-bf369efcfd79"], "manufacturer_name": ["Epic Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (42806-533-01)", "package_ndc": "42806-533-01", "marketing_start_date": "20170606"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (42806-533-10)", "package_ndc": "42806-533-10", "marketing_start_date": "20170606"}], "brand_name": "Doxepin Hydrochloride", "product_id": "42806-533_a5adf083-8dd9-4482-a3f1-589ade22b653", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "42806-533", "generic_name": "Doxepin Hydrochloride", "labeler_name": "Epic Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA210675", "marketing_category": "ANDA", "marketing_start_date": "20170606", "listing_expiration_date": "20261231"}