nortriptyline hydrochloride

Generic: nortriptyline hydrochloride

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

Drug Facts

Product Profile

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

nortriptyline hydrochloride 10 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-0810
Product ID 0093-0810_314d74dc-7394-40b9-be81-cb67b6e925a1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074132
Listing Expiration 2026-12-31
Marketing Start 1995-04-05

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00930810
Hyphenated Format 0093-0810

Supplemental Identifiers

RxCUI
198045 198046 198047 317136
UPC
0300930811012 0300930812019 0300930810015 0300930813016
UNII
00FN6IH15D

Packaging Origin

Original Packager
true

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
  • 10 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (0093-0810-01)
  • 500 CAPSULE in 1 BOTTLE (0093-0810-05)
source: ndc

Packages (2)

0093-0810-01 100 CAPSULE in 1 BOTTLE (0093-0810-01) 0093-0810-05 500 CAPSULE in 1 BOTTLE (0093-0810-05)

Ingredients (1)

nortriptyline hydrochloride (10 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": "314d74dc-7394-40b9-be81-cb67b6e925a1", "openfda": {"upc": ["0300930811012", "0300930812019", "0300930810015", "0300930813016"], "unii": ["00FN6IH15D"], "rxcui": ["198045", "198046", "198047", "317136"], "spl_set_id": ["b58d473a-b19f-4d2a-b1ae-dd398d7a29e1"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0093-0810-01)", "package_ndc": "0093-0810-01", "marketing_start_date": "19950405"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (0093-0810-05)", "package_ndc": "0093-0810-05", "marketing_start_date": "19950405"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "0093-0810_314d74dc-7394-40b9-be81-cb67b6e925a1", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "0093-0810", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nortriptyline Hydrochloride", "active_ingredients": [{"name": "NORTRIPTYLINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA074132", "marketing_category": "ANDA", "marketing_start_date": "19950405", "listing_expiration_date": "20261231"}