nortriptyline hydrochloride
Generic: nortriptyline hydrochloride
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
nortriptyline hydrochloride
Generic Name
nortriptyline hydrochloride
Labeler
american health packaging
Dosage Form
CAPSULE
Routes
Active Ingredients
nortriptyline hydrochloride 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60687-911
Product ID
60687-911_44e5c7ee-ebf1-485a-e063-6294a90acb29
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA074132
Listing Expiration
2026-12-31
Marketing Start
2025-12-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60687911
Hyphenated Format
60687-911
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 100 BLISTER PACK in 1 CARTON (60687-911-01) / 1 CAPSULE in 1 BLISTER PACK (60687-911-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "44e5c7ee-ebf1-485a-e063-6294a90acb29", "openfda": {"unii": ["00FN6IH15D"], "rxcui": ["198045", "317136"], "spl_set_id": ["d111c36d-98ed-4f0d-97ea-86fe9048deee"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-911-01) / 1 CAPSULE in 1 BLISTER PACK (60687-911-11)", "package_ndc": "60687-911-01", "marketing_start_date": "20251201"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "60687-911_44e5c7ee-ebf1-485a-e063-6294a90acb29", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "60687-911", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "American Health Packaging", "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": "20251201", "listing_expiration_date": "20261231"}