doxepin hydrochloride

Generic: doxepin hydrochloride

Labeler: redpharm drug
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxepin hydrochloride
Generic Name doxepin hydrochloride
Labeler redpharm drug
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

doxepin hydrochloride 10 mg/1

Manufacturer
Redpharm Drug

Identifiers & Regulatory

Product NDC 67296-2165
Product ID 67296-2165_45abebda-9f37-adae-e063-6294a90a811a
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 672962165
Hyphenated Format 67296-2165

Supplemental Identifiers

RxCUI
1000048
UPC
0369238117134
UNII
3U9A0FE9N5

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
  • 10 mg/1
source: ndc
Packaging
  • 20 CAPSULE in 1 BOTTLE (67296-2165-2)
source: ndc

Packages (1)

67296-2165-2 20 CAPSULE in 1 BOTTLE (67296-2165-2)

Ingredients (1)

doxepin hydrochloride (10 mg/1)

Linked Drug Pages (1)

Doxepin Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "45abebda-9f37-adae-e063-6294a90a811a", "openfda": {"upc": ["0369238117134"], "unii": ["3U9A0FE9N5"], "rxcui": ["1000048"], "spl_set_id": ["37451a61-ccb1-57b3-e063-6294a90a2592"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "20 CAPSULE in 1 BOTTLE (67296-2165-2)", "package_ndc": "67296-2165-2", "marketing_start_date": "20170628"}], "brand_name": "Doxepin Hydrochloride", "product_id": "67296-2165_45abebda-9f37-adae-e063-6294a90a811a", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "67296-2165", "generic_name": "Doxepin Hydrochloride", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA207482", "marketing_category": "ANDA", "marketing_start_date": "20170628", "listing_expiration_date": "20261231"}