doxepin hydrochloride
Generic: doxepin hydrochloride
Labeler: golden state medical supply, inc.Drug Facts
Product Profile
Brand Name
doxepin hydrochloride
Generic Name
doxepin hydrochloride
Labeler
golden state medical supply, inc.
Dosage Form
TABLET
Routes
Active Ingredients
doxepin hydrochloride 6 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51407-812
Product ID
51407-812_2a07fb40-8690-5729-e063-6294a90a4078
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA214823
Listing Expiration
2026-12-31
Marketing Start
2023-04-05
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51407812
Hyphenated Format
51407-812
Supplemental Identifiers
RxCUI
UNII
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
ANDA214823 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 6 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (51407-812-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a07fb40-8690-5729-e063-6294a90a4078", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["966787", "966793"], "spl_set_id": ["00ef7d0b-4bb9-cd5b-e063-6294a90abc35"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (51407-812-30)", "package_ndc": "51407-812-30", "marketing_start_date": "20230531"}], "brand_name": "Doxepin hydrochloride", "product_id": "51407-812_2a07fb40-8690-5729-e063-6294a90a4078", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "51407-812", "generic_name": "Doxepin hydrochloride", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "6 mg/1"}], "application_number": "ANDA214823", "marketing_category": "ANDA", "marketing_start_date": "20230405", "listing_expiration_date": "20261231"}