nortriptyline hcl

Generic: nortriptyline hcl

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nortriptyline hcl
Generic Name nortriptyline hcl
Labeler direct_rx
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

nortriptyline hydrochloride 10 mg/1

Manufacturer
Direct_rx

Identifiers & Regulatory

Product NDC 72189-563
Product ID 72189-563_1bcf2f7b-9750-54ad-e063-6394a90a28d9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA073556
Listing Expiration 2026-12-31
Marketing Start 2024-06-26

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189563
Hyphenated Format 72189-563

Supplemental Identifiers

RxCUI
198045
UNII
00FN6IH15D

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 nortriptyline hcl (source: ndc)
Generic Name nortriptyline hcl (source: ndc)
Application Number ANDA073556 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE, PLASTIC (72189-563-30)
source: ndc

Packages (1)

72189-563-30 30 CAPSULE in 1 BOTTLE, PLASTIC (72189-563-30)

Ingredients (1)

nortriptyline hydrochloride (10 mg/1)

Linked Drug Pages (1)

Nortriptyline HCL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1bcf2f7b-9750-54ad-e063-6394a90a28d9", "openfda": {"unii": ["00FN6IH15D"], "rxcui": ["198045"], "spl_set_id": ["1bcf2f7b-974f-54ad-e063-6394a90a28d9"], "manufacturer_name": ["Direct_rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (72189-563-30)", "package_ndc": "72189-563-30", "marketing_start_date": "20240626"}], "brand_name": "Nortriptyline HCL", "product_id": "72189-563_1bcf2f7b-9750-54ad-e063-6394a90a28d9", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72189-563", "generic_name": "Nortriptyline HCL", "labeler_name": "Direct_rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nortriptyline HCL", "active_ingredients": [{"name": "NORTRIPTYLINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA073556", "marketing_category": "ANDA", "marketing_start_date": "20240626", "listing_expiration_date": "20261231"}