doxepin hydrochloride

Generic: doxepin hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxepin hydrochloride
Generic Name doxepin hydrochloride
Labeler a-s medication solutions
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

doxepin hydrochloride 50 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7184
Product ID 50090-7184_7bd0f29d-ffc3-496b-9fd7-16345aa76356
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215076
Listing Expiration 2026-12-31
Marketing Start 2021-04-23

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907184
Hyphenated Format 50090-7184

Supplemental Identifiers

RxCUI
1000076
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 ANDA215076 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (50090-7184-1)
source: ndc

Packages (1)

50090-7184-1 30 CAPSULE in 1 BOTTLE (50090-7184-1)

Ingredients (1)

doxepin hydrochloride (50 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": "7bd0f29d-ffc3-496b-9fd7-16345aa76356", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000076"], "spl_set_id": ["890248d7-73b1-4ed3-b252-85775defdf34"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (50090-7184-1)", "package_ndc": "50090-7184-1", "marketing_start_date": "20240618"}], "brand_name": "DOXEPIN HYDROCHLORIDE", "product_id": "50090-7184_7bd0f29d-ffc3-496b-9fd7-16345aa76356", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "50090-7184", "generic_name": "DOXEPIN HYDROCHLORIDE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXEPIN HYDROCHLORIDE", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA215076", "marketing_category": "ANDA", "marketing_start_date": "20210423", "listing_expiration_date": "20261231"}