nortriptyline hydrochloride

Generic: nortriptyline hydrochloride

Labeler: advagen pharma ltd
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nortriptyline hydrochloride
Generic Name nortriptyline hydrochloride
Labeler advagen pharma ltd
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

nortriptyline hydrochloride 10 mg/5mL

Manufacturer
Advagen Pharma Ltd

Identifiers & Regulatory

Product NDC 72888-157
Product ID 72888-157_47ca5d0b-0a49-87d1-e063-6394a90a1edb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217731
Listing Expiration 2027-12-31
Marketing Start 2022-06-14

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72888157
Hyphenated Format 72888-157

Supplemental Identifiers

RxCUI
312036
UPC
0372888157399
UNII
00FN6IH15D

Packaging Origin

Original Packager
true

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 ANDA217731 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/5mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE (72888-157-39)
source: ndc

Packages (1)

Ingredients (1)

nortriptyline hydrochloride (10 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47ca5d0b-0a49-87d1-e063-6394a90a1edb", "openfda": {"upc": ["0372888157399"], "unii": ["00FN6IH15D"], "rxcui": ["312036"], "spl_set_id": ["bef9e24d-e730-4801-ab25-75e7d6bde225"], "manufacturer_name": ["Advagen Pharma Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (72888-157-39)", "package_ndc": "72888-157-39", "marketing_start_date": "20220614"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "72888-157_47ca5d0b-0a49-87d1-e063-6394a90a1edb", "dosage_form": "SOLUTION", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72888-157", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "Advagen Pharma Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nortriptyline Hydrochloride", "active_ingredients": [{"name": "NORTRIPTYLINE HYDROCHLORIDE", "strength": "10 mg/5mL"}], "application_number": "ANDA217731", "marketing_category": "ANDA", "marketing_start_date": "20220614", "listing_expiration_date": "20271231"}