nortriptyline hydrochloride
Generic: nortriptyline hydrochloride
Labeler: dr. reddy's laboratories inc.Drug Facts
Product Profile
Brand Name
nortriptyline hydrochloride
Generic Name
nortriptyline hydrochloride
Labeler
dr. reddy's laboratories inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
nortriptyline hydrochloride 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
75907-070
Product ID
75907-070_8630467c-de24-9d2e-ac96-ce9afeaca9b1
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA073556
Listing Expiration
2026-12-31
Marketing Start
2023-11-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
75907070
Hyphenated Format
75907-070
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE, PLASTIC (75907-070-01)
- 500 CAPSULE in 1 BOTTLE, PLASTIC (75907-070-05)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8630467c-de24-9d2e-ac96-ce9afeaca9b1", "openfda": {"unii": ["00FN6IH15D"], "rxcui": ["198045", "198046", "198047", "317136"], "spl_set_id": ["b1d9582c-742c-91a8-c2b3-bbdb21220470"], "manufacturer_name": ["Dr. Reddy's Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE, PLASTIC (75907-070-01)", "package_ndc": "75907-070-01", "marketing_start_date": "20231117"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE, PLASTIC (75907-070-05)", "package_ndc": "75907-070-05", "marketing_start_date": "20231117"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "75907-070_8630467c-de24-9d2e-ac96-ce9afeaca9b1", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "75907-070", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "Dr. Reddy's Laboratories 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": "20231117", "listing_expiration_date": "20261231"}