sertraline
Generic: sertraline
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
sertraline
Generic Name
sertraline
Labeler
a-s medication solutions
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
sertraline hydrochloride 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-7295
Product ID
50090-7295_c2e94e89-6016-4a0f-be9a-6eee53257a72
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
500907295
Hyphenated Format
50090-7295
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 (source: ndc)
Generic Name
sertraline (source: ndc)
Application Number
ANDA077670 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 90 TABLET, FILM COATED in 1 BOTTLE (50090-7295-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c2e94e89-6016-4a0f-be9a-6eee53257a72", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312938"], "spl_set_id": ["f5bf9595-d9f9-40b1-9b3b-da277fd5ab7f"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7295-0)", "package_ndc": "50090-7295-0", "marketing_start_date": "20241010"}], "brand_name": "Sertraline", "product_id": "50090-7295_c2e94e89-6016-4a0f-be9a-6eee53257a72", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-7295", "generic_name": "Sertraline", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sertraline", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA077670", "marketing_category": "ANDA", "marketing_start_date": "20070206", "listing_expiration_date": "20261231"}