nortriptyline hydrochloride

Generic: nortriptyline hydrochloride

Labeler: st. mary's medical park pharmacy
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nortriptyline hydrochloride
Generic Name nortriptyline hydrochloride
Labeler st. mary's medical park pharmacy
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

nortriptyline hydrochloride 10 mg/1

Manufacturer
ST. MARY'S MEDICAL PARK PHARMACY

Identifiers & Regulatory

Product NDC 60760-908
Product ID 60760-908_4471fe47-2acd-41a4-e063-6294a90a755b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA073556
Listing Expiration 2026-12-31
Marketing Start 2023-11-17

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60760908
Hyphenated Format 60760-908

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

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 60 CAPSULE in 1 BOTTLE, PLASTIC (60760-908-60)
source: ndc

Packages (1)

Ingredients (1)

nortriptyline hydrochloride (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4471fe47-2acd-41a4-e063-6294a90a755b", "openfda": {"unii": ["00FN6IH15D"], "rxcui": ["198045"], "spl_set_id": ["21770082-7a99-520d-e063-6394a90ab9cb"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE, PLASTIC (60760-908-60)", "package_ndc": "60760-908-60", "marketing_start_date": "20240828"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "60760-908_4471fe47-2acd-41a4-e063-6294a90a755b", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "60760-908", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nortriptyline Hydrochloride", "active_ingredients": [{"name": "NORTRIPTYLINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA073556", "marketing_category": "ANDA", "marketing_start_date": "20231117", "listing_expiration_date": "20261231"}