doxepin hydrochloride

Generic: doxepin hydrochloride

Labeler: contract pharmacal corp.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxepin hydrochloride
Generic Name doxepin hydrochloride
Labeler contract pharmacal corp.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

doxepin hydrochloride 75 mg/1

Manufacturer
Contract Pharmacal Corp.

Identifiers & Regulatory

Product NDC 10267-5062
Product ID 10267-5062_abbf7078-a013-4e1a-e053-2995a90a792d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213474
Listing Expiration 2026-12-31
Marketing Start 2021-01-24

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 102675062
Hyphenated Format 10267-5062

Supplemental Identifiers

RxCUI
1000048 1000058 1000070 1000076 1000097
UPC
0310267506390
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 ANDA213474 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 1000 CAPSULE in 1 BOTTLE (10267-5062-4)
  • 90 CAPSULE in 1 BOTTLE (10267-5062-9)
source: ndc

Packages (2)

10267-5062-4 1000 CAPSULE in 1 BOTTLE (10267-5062-4) 10267-5062-9 90 CAPSULE in 1 BOTTLE (10267-5062-9)

Ingredients (1)

doxepin hydrochloride (75 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": "abbf7078-a013-4e1a-e053-2995a90a792d", "openfda": {"upc": ["0310267506390"], "unii": ["3U9A0FE9N5"], "rxcui": ["1000048", "1000058", "1000070", "1000076", "1000097"], "spl_set_id": ["abbf7078-a012-4e1a-e053-2995a90a792d"], "manufacturer_name": ["Contract Pharmacal Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (10267-5062-4)", "package_ndc": "10267-5062-4", "marketing_start_date": "20210124"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (10267-5062-9)", "package_ndc": "10267-5062-9", "marketing_start_date": "20210124"}], "brand_name": "Doxepin Hydrochloride", "product_id": "10267-5062_abbf7078-a013-4e1a-e053-2995a90a792d", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "10267-5062", "generic_name": "Doxepin Hydrochloride", "labeler_name": "Contract Pharmacal Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA213474", "marketing_category": "ANDA", "marketing_start_date": "20210124", "listing_expiration_date": "20261231"}