nortriptyline hydrochloride

Generic: nortriptyline hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nortriptyline hydrochloride
Generic Name nortriptyline hydrochloride
Labeler a-s medication solutions
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

nortriptyline hydrochloride 50 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-1322
Product ID 50090-1322_ca48b9c4-5ac7-47e9-90fd-157b40c0cfc5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074132
Listing Expiration 2026-12-31
Marketing Start 1995-04-05

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500901322
Hyphenated Format 50090-1322

Supplemental Identifiers

RxCUI
198046
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 ANDA074132 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 90 CAPSULE in 1 BOTTLE (50090-1322-0)
source: ndc

Packages (1)

50090-1322-0 90 CAPSULE in 1 BOTTLE (50090-1322-0)

Ingredients (1)

nortriptyline hydrochloride (50 mg/1)

Linked Drug Pages (1)

Nortriptyline Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ca48b9c4-5ac7-47e9-90fd-157b40c0cfc5", "openfda": {"unii": ["00FN6IH15D"], "rxcui": ["198046"], "spl_set_id": ["a2cf7783-7019-49ea-ab55-796674d94546"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (50090-1322-0)", "package_ndc": "50090-1322-0", "marketing_start_date": "20141128"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "50090-1322_ca48b9c4-5ac7-47e9-90fd-157b40c0cfc5", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "50090-1322", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nortriptyline Hydrochloride", "active_ingredients": [{"name": "NORTRIPTYLINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA074132", "marketing_category": "ANDA", "marketing_start_date": "19950405", "listing_expiration_date": "20261231"}