doxepin hydrochloride (72205-092)

Drug Facts

Product Profile

Brand Name doxepin hydrochloride

Generic Name doxepin hydrochloride

Labeler novadoz pharmaceuticals llc

Dosage Form CAPSULE

Routes

ORAL

Active Ingredients

doxepin hydrochloride 100 mg/1

Manufacturer

Novadoz Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 72205-092

Product ID 72205-092_2b1f0144-65d8-451f-8054-6be1675f102c

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA215113

Listing Expiration 2026-12-31

Marketing Start 2022-06-27

Pharmacologic Class

Classes

tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72205092

Hyphenated Format 72205-092

Supplemental Identifiers

RxCUI

1000048 1000058 1000070 1000076 1000097

UPC

0372205092990 0372205088917 0372205090996 0372205089990 0372205088993 0372205089914 0372205092914 0372205091917 0372205091993 0372205090910

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 ANDA215113 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

100 mg/1

source: ndc

Packaging

100 CAPSULE in 1 BOTTLE, PLASTIC (72205-092-91)
1000 CAPSULE in 1 BOTTLE, PLASTIC (72205-092-99)

source: ndc

Packages (2)

72205-092-91 100 CAPSULE in 1 BOTTLE, PLASTIC (72205-092-91) 72205-092-99 1000 CAPSULE in 1 BOTTLE, PLASTIC (72205-092-99)

Ingredients (1)

doxepin hydrochloride (100 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": "2b1f0144-65d8-451f-8054-6be1675f102c", "openfda": {"upc": ["0372205092990", "0372205088917", "0372205090996", "0372205089990", "0372205088993", "0372205089914", "0372205092914", "0372205091917", "0372205091993", "0372205090910"], "unii": ["3U9A0FE9N5"], "rxcui": ["1000048", "1000058", "1000070", "1000076", "1000097"], "spl_set_id": ["2b1f0144-65d8-451f-8054-6be1675f102c"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE, PLASTIC (72205-092-91)", "package_ndc": "72205-092-91", "marketing_start_date": "20220627"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE, PLASTIC (72205-092-99)", "package_ndc": "72205-092-99", "marketing_start_date": "20220627"}], "brand_name": "Doxepin Hydrochloride", "product_id": "72205-092_2b1f0144-65d8-451f-8054-6be1675f102c", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72205-092", "generic_name": "Doxepin Hydrochloride", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA215113", "marketing_category": "ANDA", "marketing_start_date": "20220627", "listing_expiration_date": "20261231"}