prudoxin
Generic: doxepin hydrochloride
Labeler: mylan pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
prudoxin
Generic Name
doxepin hydrochloride
Labeler
mylan pharmaceuticals inc.
Dosage Form
CREAM
Routes
Active Ingredients
doxepin hydrochloride 50 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
0378-8130
Product ID
0378-8130_dc5b7069-dc63-4393-bd87-2828328103b0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA020126
Listing Expiration
2026-12-31
Marketing Start
2018-08-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03788130
Hyphenated Format
0378-8130
Supplemental Identifiers
RxCUI
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
prudoxin (source: ndc)
Generic Name
doxepin hydrochloride (source: ndc)
Application Number
NDA020126 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/g
Packaging
- 1 TUBE in 1 CARTON (0378-8130-45) / 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": "dc5b7069-dc63-4393-bd87-2828328103b0", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000091", "1000093"], "spl_set_id": ["ca53346b-8ab3-4722-98f6-cf272706d3fa"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (0378-8130-45) / 45 g in 1 TUBE", "package_ndc": "0378-8130-45", "marketing_start_date": "20180801"}], "brand_name": "PRUDOXIN", "product_id": "0378-8130_dc5b7069-dc63-4393-bd87-2828328103b0", "dosage_form": "CREAM", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "0378-8130", "generic_name": "doxepin hydrochloride", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRUDOXIN", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "50 mg/g"}], "application_number": "NDA020126", "marketing_category": "NDA", "marketing_start_date": "20180801", "listing_expiration_date": "20261231"}