doxepin hydrochloride

Generic: doxepin hydrochloride

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

Drug Facts

Product Profile

Brand Name doxepin hydrochloride
Generic Name doxepin hydrochloride
Labeler endo usa, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

doxepin hydrochloride 150 mg/1

Manufacturer
Endo USA, Inc.

Identifiers & Regulatory

Product NDC 49884-222
Product ID 49884-222_75a2a220-95ff-4c6a-aa58-15e3352b6e7f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071422
Listing Expiration 2026-12-31
Marketing Start 1987-11-09

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 49884222
Hyphenated Format 49884-222

Supplemental Identifiers

RxCUI
1000064
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 ANDA071422 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (49884-222-01)
  • 50 CAPSULE in 1 BOTTLE (49884-222-03)
  • 500 CAPSULE in 1 BOTTLE (49884-222-05)
source: ndc

Packages (3)

49884-222-01 100 CAPSULE in 1 BOTTLE (49884-222-01) 49884-222-03 50 CAPSULE in 1 BOTTLE (49884-222-03) 49884-222-05 500 CAPSULE in 1 BOTTLE (49884-222-05)

Ingredients (1)

doxepin hydrochloride (150 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": "75a2a220-95ff-4c6a-aa58-15e3352b6e7f", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000064"], "spl_set_id": ["71cff7cd-0410-4194-9cdd-af404a869edd"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (49884-222-01)", "package_ndc": "49884-222-01", "marketing_start_date": "19871109"}, {"sample": false, "description": "50 CAPSULE in 1 BOTTLE (49884-222-03)", "package_ndc": "49884-222-03", "marketing_start_date": "19871109"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (49884-222-05)", "package_ndc": "49884-222-05", "marketing_start_date": "19871109"}], "brand_name": "Doxepin Hydrochloride", "product_id": "49884-222_75a2a220-95ff-4c6a-aa58-15e3352b6e7f", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "49884-222", "generic_name": "Doxepin Hydrochloride", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA071422", "marketing_category": "ANDA", "marketing_start_date": "19871109", "listing_expiration_date": "20261231"}