nortriptyline hydrochloride

Generic: nortriptyline hydrochloride

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

nortriptyline hydrochloride 25 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-722
Product ID 43063-722_414b1374-fc77-1888-e063-6394a90ad253
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA073556
Listing Expiration 2026-12-31
Marketing Start 2016-06-01

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43063722
Hyphenated Format 43063-722

Supplemental Identifiers

RxCUI
317136
UPC
0343063722305
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 ANDA073556 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE, PLASTIC (43063-722-30)
source: ndc

Packages (1)

43063-722-30 30 CAPSULE in 1 BOTTLE, PLASTIC (43063-722-30)

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": "414b1374-fc77-1888-e063-6394a90ad253", "openfda": {"upc": ["0343063722305"], "unii": ["00FN6IH15D"], "rxcui": ["317136"], "spl_set_id": ["ba4edb34-82ac-4c98-8abd-fd6176838c78"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (43063-722-30)", "package_ndc": "43063-722-30", "marketing_start_date": "20161027"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "43063-722_414b1374-fc77-1888-e063-6394a90ad253", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "43063-722", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nortriptyline Hydrochloride", "active_ingredients": [{"name": "NORTRIPTYLINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA073556", "marketing_category": "ANDA", "marketing_start_date": "20160601", "listing_expiration_date": "20261231"}