nortriptyline hydrochloride

Generic: nortriptyline hydrochloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nortriptyline hydrochloride
Generic Name nortriptyline hydrochloride
Labeler proficient rx lp
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

nortriptyline hydrochloride 75 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-809
Product ID 63187-809_3bc803bf-606e-4857-a8a6-1a33740d35c5
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 63187809
Hyphenated Format 63187-809

Supplemental Identifiers

RxCUI
198047
UPC
0363187809300
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
  • 75 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (63187-809-00)
  • 30 CAPSULE in 1 BOTTLE (63187-809-30)
  • 60 CAPSULE in 1 BOTTLE (63187-809-60)
  • 90 CAPSULE in 1 BOTTLE (63187-809-90)
source: ndc

Packages (4)

Ingredients (1)

nortriptyline hydrochloride (75 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3bc803bf-606e-4857-a8a6-1a33740d35c5", "openfda": {"upc": ["0363187809300"], "unii": ["00FN6IH15D"], "rxcui": ["198047"], "spl_set_id": ["2f9fc7a0-163a-4a05-84a7-7999a41ecb1f"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (63187-809-00)", "package_ndc": "63187-809-00", "marketing_start_date": "20170201"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (63187-809-30)", "package_ndc": "63187-809-30", "marketing_start_date": "20170201"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (63187-809-60)", "package_ndc": "63187-809-60", "marketing_start_date": "20170201"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (63187-809-90)", "package_ndc": "63187-809-90", "marketing_start_date": "20170201"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "63187-809_3bc803bf-606e-4857-a8a6-1a33740d35c5", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "63187-809", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nortriptyline Hydrochloride", "active_ingredients": [{"name": "NORTRIPTYLINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA074132", "marketing_category": "ANDA", "marketing_start_date": "19950405", "listing_expiration_date": "20261231"}