Nortriptyline Hydrochloride

Generic: Nortriptyline Hydrochloride

Labeler: REMEDYREPACK INC.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Active

Drug Facts

Product Profile

Brand Name Nortriptyline Hydrochloride
Generic Name Nortriptyline Hydrochloride
Labeler REMEDYREPACK INC.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

NORTRIPTYLINE HYDROCHLORIDE 75 mg/1

Identifiers & Regulatory

Product NDC 70518-4067
Product ID 70518-4067_3fa2dd80-c864-6411-e063-6294a90ad9f7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074132
Listing Expiration 2026-12-31
Marketing Start 2024-05-05

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184067
Hyphenated Format 70518-4067

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
  • 30 CAPSULE in 1 BLISTER PACK (70518-4067-0)
source: ndc

Packages (1)

70518-4067-0 30 CAPSULE in 1 BLISTER PACK (70518-4067-0)

Ingredients (1)

NORTRIPTYLINE HYDROCHLORIDE (75 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": "3fa2dd80-c864-6411-e063-6294a90ad9f7", "openfda": {"unii": ["00FN6IH15D"], "rxcui": ["198047"], "spl_set_id": ["c0bf77c7-e53a-4529-b1f0-a30feb8b168d"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-4067-0)", "package_ndc": "70518-4067-0", "marketing_start_date": "20240505"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "70518-4067_3fa2dd80-c864-6411-e063-6294a90ad9f7", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-4067", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "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": "20240505", "listing_expiration_date": "20261231"}