doxepin hydrochloride

Generic: doxepin hydrochloride

Labeler: amneal pharmaceuticals ny llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxepin hydrochloride
Generic Name doxepin hydrochloride
Labeler amneal pharmaceuticals ny llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

doxepin hydrochloride 100 mg/1

Manufacturer
Amneal Pharmaceuticals NY LLC

Identifiers & Regulatory

Product NDC 69238-1173
Product ID 69238-1173_0d905a6d-9f40-435d-a39a-f97ce7264b15
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207482
Listing Expiration 2026-12-31
Marketing Start 2017-06-28

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 692381173
Hyphenated Format 69238-1173

Supplemental Identifiers

RxCUI
1000048 1000058 1000070 1000076 1000097
UPC
0369238117134
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 ANDA207482 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 1000 CAPSULE in 1 BOTTLE (69238-1173-1)
  • 30 CAPSULE in 1 BOTTLE (69238-1173-3)
  • 90 CAPSULE in 1 BOTTLE (69238-1173-9)
source: ndc

Packages (3)

Ingredients (1)

doxepin hydrochloride (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0d905a6d-9f40-435d-a39a-f97ce7264b15", "openfda": {"upc": ["0369238117134"], "unii": ["3U9A0FE9N5"], "rxcui": ["1000048", "1000058", "1000070", "1000076", "1000097"], "spl_set_id": ["20bfb8af-7933-4e5c-a2b5-010659d9125b"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (69238-1173-1)", "package_ndc": "69238-1173-1", "marketing_start_date": "20170628"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (69238-1173-3)", "package_ndc": "69238-1173-3", "marketing_start_date": "20170628"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (69238-1173-9)", "package_ndc": "69238-1173-9", "marketing_start_date": "20170628"}], "brand_name": "Doxepin Hydrochloride", "product_id": "69238-1173_0d905a6d-9f40-435d-a39a-f97ce7264b15", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "69238-1173", "generic_name": "Doxepin Hydrochloride", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA207482", "marketing_category": "ANDA", "marketing_start_date": "20170628", "listing_expiration_date": "20261231"}