nortriptyline hydrochloride

Generic: nortriptyline hydrochloride

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nortriptyline hydrochloride
Generic Name nortriptyline hydrochloride
Labeler northwind health company, llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

nortriptyline hydrochloride 25 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-507
Product ID 51655-507_490f8fd3-7543-fb69-e063-6294a90a8b21
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075520
Listing Expiration 2027-12-31
Marketing Start 2021-01-13

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51655507
Hyphenated Format 51655-507

Supplemental Identifiers

RxCUI
317136
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 hydrochloride (source: ndc)
Generic Name nortriptyline hydrochloride (source: ndc)
Application Number ANDA075520 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE, PLASTIC (51655-507-52)
source: ndc

Packages (1)

Ingredients (1)

nortriptyline hydrochloride (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "490f8fd3-7543-fb69-e063-6294a90a8b21", "openfda": {"unii": ["00FN6IH15D"], "rxcui": ["317136"], "spl_set_id": ["dae3314f-3128-787f-e053-2995a90aff19"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (51655-507-52)", "package_ndc": "51655-507-52", "marketing_start_date": "20210113"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "51655-507_490f8fd3-7543-fb69-e063-6294a90a8b21", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "51655-507", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nortriptyline Hydrochloride", "active_ingredients": [{"name": "NORTRIPTYLINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA075520", "marketing_category": "ANDA", "marketing_start_date": "20210113", "listing_expiration_date": "20271231"}