doxepin hydrochloride

Generic: doxepin hydrochloride

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxepin hydrochloride
Generic Name doxepin hydrochloride
Labeler teva pharmaceuticals usa, inc.
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

doxepin hydrochloride 50 mg/g

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-9609
Product ID 0093-9609_7d22a419-3d33-492c-b054-fb29a82ce643
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215408
Listing Expiration 2026-12-31
Marketing Start 2023-02-17

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00939609
Hyphenated Format 0093-9609

Supplemental Identifiers

RxCUI
1000091
UPC
0300939609955
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 ANDA215408 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (0093-9609-95) / 45 g in 1 TUBE
source: ndc

Packages (1)

Ingredients (1)

doxepin hydrochloride (50 mg/g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "7d22a419-3d33-492c-b054-fb29a82ce643", "openfda": {"upc": ["0300939609955"], "unii": ["3U9A0FE9N5"], "rxcui": ["1000091"], "spl_set_id": ["4a4eab1c-8e19-48f5-9216-09ab83eaa5f8"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (0093-9609-95)  / 45 g in 1 TUBE", "package_ndc": "0093-9609-95", "marketing_start_date": "20230217"}], "brand_name": "doxepin hydrochloride", "product_id": "0093-9609_7d22a419-3d33-492c-b054-fb29a82ce643", "dosage_form": "CREAM", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "0093-9609", "generic_name": "doxepin hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "doxepin hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "50 mg/g"}], "application_number": "ANDA215408", "marketing_category": "ANDA", "marketing_start_date": "20230217", "listing_expiration_date": "20261231"}