doxepin hydrochloride
Generic: doxepin hydrochloride
Labeler: teva pharmaceuticals usa, inc.Drug Facts
Product Profile
Brand Name
doxepin hydrochloride
Generic Name
doxepin hydrochloride
Labeler
teva pharmaceuticals usa, inc.
Dosage Form
CREAM
Routes
Active Ingredients
doxepin hydrochloride 50 mg/g
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00939609
Hyphenated Format
0093-9609
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 50 mg/g
Packaging
- 1 TUBE in 1 CARTON (0093-9609-95) / 45 g in 1 TUBE
Packages (1)
Ingredients (1)
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"}