sertraline hydrochloride
Generic: sertraline hydrochloride
Labeler: major pharmaceuticalsDrug Facts
Product Profile
Brand Name
sertraline hydrochloride
Generic Name
sertraline hydrochloride
Labeler
major pharmaceuticals
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
sertraline hydrochloride 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0904-6924
Product ID
0904-6924_e586e0c5-ace8-4575-a549-f4c85a351653
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077670
Listing Expiration
2026-12-31
Marketing Start
2007-02-06
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09046924
Hyphenated Format
0904-6924
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
sertraline hydrochloride (source: ndc)
Generic Name
sertraline hydrochloride (source: ndc)
Application Number
ANDA077670 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 100 BLISTER PACK in 1 CARTON (0904-6924-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e586e0c5-ace8-4575-a549-f4c85a351653", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312938", "312940", "312941"], "spl_set_id": ["4cf8d5c8-842b-4e7c-9a99-3f41ef8abbdb"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6924-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6924-61", "marketing_start_date": "20070206"}], "brand_name": "Sertraline Hydrochloride", "product_id": "0904-6924_e586e0c5-ace8-4575-a549-f4c85a351653", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "0904-6924", "generic_name": "Sertraline Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sertraline Hydrochloride", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA077670", "marketing_category": "ANDA", "marketing_start_date": "20070206", "listing_expiration_date": "20261231"}