nortriptyline hydrochloride

Generic: nortriptyline hydrochloride

Labeler: nucare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nortriptyline hydrochloride
Generic Name nortriptyline hydrochloride
Labeler nucare pharmaceuticals, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

nortriptyline hydrochloride 25 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3211
Product ID 68071-3211_1da1201b-5eff-2f85-e063-6294a90a969c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075520
Listing Expiration 2026-12-31
Marketing Start 2000-05-08

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713211
Hyphenated Format 68071-3211

Supplemental Identifiers

RxCUI
317136
UPC
0368071321135
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 ANDA075520 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 120 CAPSULE in 1 BOTTLE (68071-3211-1)
  • 20 CAPSULE in 1 BOTTLE (68071-3211-2)
  • 30 CAPSULE in 1 BOTTLE (68071-3211-3)
  • 45 CAPSULE in 1 BOTTLE (68071-3211-5)
  • 60 CAPSULE in 1 BOTTLE (68071-3211-6)
  • 90 CAPSULE in 1 BOTTLE (68071-3211-9)
source: ndc

Packages (6)

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": "1da1201b-5eff-2f85-e063-6294a90a969c", "openfda": {"upc": ["0368071321135"], "unii": ["00FN6IH15D"], "rxcui": ["317136"], "spl_set_id": ["51778813-0ec1-6b4f-e054-00144ff8d46c"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "120 CAPSULE in 1 BOTTLE (68071-3211-1)", "package_ndc": "68071-3211-1", "marketing_start_date": "20170608"}, {"sample": false, "description": "20 CAPSULE in 1 BOTTLE (68071-3211-2)", "package_ndc": "68071-3211-2", "marketing_start_date": "20170608"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68071-3211-3)", "package_ndc": "68071-3211-3", "marketing_start_date": "20170608"}, {"sample": false, "description": "45 CAPSULE in 1 BOTTLE (68071-3211-5)", "package_ndc": "68071-3211-5", "marketing_start_date": "20170608"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (68071-3211-6)", "package_ndc": "68071-3211-6", "marketing_start_date": "20170608"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (68071-3211-9)", "package_ndc": "68071-3211-9", "marketing_start_date": "20170608"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "68071-3211_1da1201b-5eff-2f85-e063-6294a90a969c", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "68071-3211", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nortriptyline Hydrochloride", "active_ingredients": [{"name": "NORTRIPTYLINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA075520", "marketing_category": "ANDA", "marketing_start_date": "20000508", "listing_expiration_date": "20261231"}