nortriptyline hydrochloride
Generic: nortriptyline hydrochloride
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
nortriptyline hydrochloride
Generic Name
nortriptyline hydrochloride
Labeler
proficient rx lp
Dosage Form
CAPSULE
Routes
Active Ingredients
nortriptyline hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71205-770
Product ID
71205-770_30263e15-de21-4db4-aceb-59d619909e82
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA074132
Listing Expiration
2026-12-31
Marketing Start
1995-04-05
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71205770
Hyphenated Format
71205-770
Supplemental Identifiers
RxCUI
UPC
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
- 10 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE (71205-770-30)
- 60 CAPSULE in 1 BOTTLE (71205-770-60)
- 90 CAPSULE in 1 BOTTLE (71205-770-90)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "30263e15-de21-4db4-aceb-59d619909e82", "openfda": {"upc": ["0371205770303"], "unii": ["00FN6IH15D"], "rxcui": ["198045"], "spl_set_id": ["30263e15-de21-4db4-aceb-59d619909e82"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (71205-770-30)", "package_ndc": "71205-770-30", "marketing_start_date": "20230310"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (71205-770-60)", "package_ndc": "71205-770-60", "marketing_start_date": "20230310"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (71205-770-90)", "package_ndc": "71205-770-90", "marketing_start_date": "20230310"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "71205-770_30263e15-de21-4db4-aceb-59d619909e82", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "71205-770", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "Proficient Rx LP", "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"}