nortriptyline hydrochloride

Generic: nortriptyline hydrochloride

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nortriptyline hydrochloride
Generic Name nortriptyline hydrochloride
Labeler american health packaging
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

nortriptyline hydrochloride 25 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-911
Product ID 60687-911_44e5c7ee-ebf1-485a-e063-6294a90acb29
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074132
Listing Expiration 2026-12-31
Marketing Start 2025-12-01

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687911
Hyphenated Format 60687-911

Supplemental Identifiers

RxCUI
198045 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 ANDA074132 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (60687-911-01) / 1 CAPSULE in 1 BLISTER PACK (60687-911-11)
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": "44e5c7ee-ebf1-485a-e063-6294a90acb29", "openfda": {"unii": ["00FN6IH15D"], "rxcui": ["198045", "317136"], "spl_set_id": ["d111c36d-98ed-4f0d-97ea-86fe9048deee"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-911-01)  / 1 CAPSULE in 1 BLISTER PACK (60687-911-11)", "package_ndc": "60687-911-01", "marketing_start_date": "20251201"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "60687-911_44e5c7ee-ebf1-485a-e063-6294a90acb29", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "60687-911", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nortriptyline Hydrochloride", "active_ingredients": [{"name": "NORTRIPTYLINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA074132", "marketing_category": "ANDA", "marketing_start_date": "20251201", "listing_expiration_date": "20261231"}