nortriptyline hydrochloride

Generic: nortriptyline hydrochloride

Labeler: direct rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

nortriptyline hydrochloride 25 mg/1

Manufacturer
Direct Rx

Identifiers & Regulatory

Product NDC 61919-171
Product ID 61919-171_48468ca6-013d-3ee8-e063-6294a90a61c9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074132
Listing Expiration 2027-12-31
Marketing Start 2015-01-01

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 61919171
Hyphenated Format 61919-171

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
  • 30 CAPSULE in 1 BOTTLE (61919-171-30)
  • 60 BOTTLE in 1 BOTTLE (61919-171-60) / 30 CAPSULE in 1 BOTTLE (61919-171-30)
source: ndc

Packages (2)

61919-171-30 30 CAPSULE in 1 BOTTLE (61919-171-30) 61919-171-60 60 BOTTLE in 1 BOTTLE (61919-171-60) / 30 CAPSULE in 1 BOTTLE (61919-171-30)

Ingredients (1)

nortriptyline hydrochloride (25 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": "48468ca6-013d-3ee8-e063-6294a90a61c9", "openfda": {"unii": ["00FN6IH15D"], "rxcui": ["198045", "317136"], "spl_set_id": ["017f7717-e160-4142-9a5a-1a2bd9776707"], "manufacturer_name": ["Direct Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (61919-171-30)", "package_ndc": "61919-171-30", "marketing_start_date": "20150101"}, {"sample": false, "description": "60 BOTTLE in 1 BOTTLE (61919-171-60)  / 30 CAPSULE in 1 BOTTLE (61919-171-30)", "package_ndc": "61919-171-60", "marketing_start_date": "20250806"}], "brand_name": "NORTRIPTYLINE HYDROCHLORIDE", "product_id": "61919-171_48468ca6-013d-3ee8-e063-6294a90a61c9", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "61919-171", "generic_name": "NORTRIPTYLINE HYDROCHLORIDE", "labeler_name": "Direct Rx", "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": "20150101", "listing_expiration_date": "20271231"}