DOXEPIN HYDROCHLORIDE

Generic: DOXEPIN HYDROCHLORIDE

Labeler: NuCare Pharmaceuticals,Inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Active

Drug Facts

Product Profile

Brand Name DOXEPIN HYDROCHLORIDE
Generic Name DOXEPIN HYDROCHLORIDE
Labeler NuCare Pharmaceuticals,Inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

DOXEPIN HYDROCHLORIDE 10 mg/1

Identifiers & Regulatory

Product NDC 68071-2356
Product ID 68071-2356_2b5c46fa-bfd7-c890-e063-6294a90a8759
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213063
Listing Expiration 2026-12-31
Marketing Start 2020-07-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680712356
Hyphenated Format 68071-2356

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 ANDA213063 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (68071-2356-1)
source: ndc

Packages (1)

68071-2356-1 100 CAPSULE in 1 BOTTLE (68071-2356-1)

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": "2b5c46fa-bfd7-c890-e063-6294a90a8759", "openfda": {"upc": ["0368071235616"], "unii": ["3U9A0FE9N5"], "rxcui": ["1000048"], "spl_set_id": ["bd0a04e2-cd1d-bd3f-e053-2995a90a7c81"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (68071-2356-1)", "package_ndc": "68071-2356-1", "marketing_start_date": "20210308"}], "brand_name": "DOXEPIN HYDROCHLORIDE", "product_id": "68071-2356_2b5c46fa-bfd7-c890-e063-6294a90a8759", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "68071-2356", "generic_name": "DOXEPIN HYDROCHLORIDE", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXEPIN HYDROCHLORIDE", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA213063", "marketing_category": "ANDA", "marketing_start_date": "20200701", "listing_expiration_date": "20261231"}