sertraline hydrochloride
Generic: sertraline hydrochloride
Labeler: aurobindo pharma limitedDrug Facts
Product Profile
Brand Name
sertraline hydrochloride
Generic Name
sertraline hydrochloride
Labeler
aurobindo pharma limited
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
sertraline hydrochloride 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
65862-012
Product ID
65862-012_50d67885-52a9-49a4-9f2a-f82749747222
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077206
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
65862012
Hyphenated Format
65862-012
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
sertraline hydrochloride (source: ndc)
Generic Name
sertraline hydrochloride (source: ndc)
Application Number
ANDA077206 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 100 TABLET, FILM COATED in 1 BOTTLE (65862-012-01)
- 500 TABLET, FILM COATED in 1 BOTTLE (65862-012-05)
- 30 TABLET, FILM COATED in 1 BOTTLE (65862-012-30)
- 50 TABLET, FILM COATED in 1 BOTTLE (65862-012-50)
- 5000 TABLET, FILM COATED in 1 BOTTLE (65862-012-51)
- 60 TABLET, FILM COATED in 1 BOTTLE (65862-012-60)
- 90 TABLET, FILM COATED in 1 BOTTLE (65862-012-90)
- 1000 TABLET, FILM COATED in 1 BOTTLE (65862-012-99)
Packages (8)
65862-012-01
100 TABLET, FILM COATED in 1 BOTTLE (65862-012-01)
65862-012-05
500 TABLET, FILM COATED in 1 BOTTLE (65862-012-05)
65862-012-30
30 TABLET, FILM COATED in 1 BOTTLE (65862-012-30)
65862-012-50
50 TABLET, FILM COATED in 1 BOTTLE (65862-012-50)
65862-012-51
5000 TABLET, FILM COATED in 1 BOTTLE (65862-012-51)
65862-012-60
60 TABLET, FILM COATED in 1 BOTTLE (65862-012-60)
65862-012-90
90 TABLET, FILM COATED in 1 BOTTLE (65862-012-90)
65862-012-99
1000 TABLET, FILM COATED in 1 BOTTLE (65862-012-99)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "50d67885-52a9-49a4-9f2a-f82749747222", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312938", "312940", "312941"], "spl_set_id": ["39a85db1-9e59-4ab0-9e18-36757f019faa"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65862-012-01)", "package_ndc": "65862-012-01", "marketing_start_date": "20070206"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65862-012-05)", "package_ndc": "65862-012-05", "marketing_start_date": "20070206"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65862-012-30)", "package_ndc": "65862-012-30", "marketing_start_date": "20070206"}, {"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (65862-012-50)", "package_ndc": "65862-012-50", "marketing_start_date": "20070206"}, {"sample": false, "description": "5000 TABLET, FILM COATED in 1 BOTTLE (65862-012-51)", "package_ndc": "65862-012-51", "marketing_start_date": "20070206"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (65862-012-60)", "package_ndc": "65862-012-60", "marketing_start_date": "20070206"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65862-012-90)", "package_ndc": "65862-012-90", "marketing_start_date": "20070206"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65862-012-99)", "package_ndc": "65862-012-99", "marketing_start_date": "20070206"}], "brand_name": "Sertraline Hydrochloride", "product_id": "65862-012_50d67885-52a9-49a4-9f2a-f82749747222", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "65862-012", "generic_name": "Sertraline Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sertraline Hydrochloride", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA077206", "marketing_category": "ANDA", "marketing_start_date": "20070206", "listing_expiration_date": "20261231"}