sertraline hydrochloride
Generic: sertraline hydrochloride
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
sertraline hydrochloride
Generic Name
sertraline hydrochloride
Labeler
nucare pharmaceuticals,inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
sertraline hydrochloride 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-4494
Product ID
68071-4494_1a8d9cca-7c68-1e64-e063-6294a90a74bd
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
680714494
Hyphenated Format
68071-4494
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
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
- 20 TABLET, FILM COATED in 1 BOTTLE (68071-4494-2)
- 30 TABLET, FILM COATED in 1 BOTTLE (68071-4494-3)
- 56 TABLET, FILM COATED in 1 BOTTLE (68071-4494-5)
- 60 TABLET, FILM COATED in 1 BOTTLE (68071-4494-6)
- 28 TABLET, FILM COATED in 1 BOTTLE (68071-4494-8)
- 90 TABLET, FILM COATED in 1 BOTTLE (68071-4494-9)
Packages (6)
68071-4494-2
20 TABLET, FILM COATED in 1 BOTTLE (68071-4494-2)
68071-4494-3
30 TABLET, FILM COATED in 1 BOTTLE (68071-4494-3)
68071-4494-5
56 TABLET, FILM COATED in 1 BOTTLE (68071-4494-5)
68071-4494-6
60 TABLET, FILM COATED in 1 BOTTLE (68071-4494-6)
68071-4494-8
28 TABLET, FILM COATED in 1 BOTTLE (68071-4494-8)
68071-4494-9
90 TABLET, FILM COATED in 1 BOTTLE (68071-4494-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1a8d9cca-7c68-1e64-e063-6294a90a74bd", "openfda": {"upc": ["0368071449495"], "unii": ["UTI8907Y6X"], "rxcui": ["312941"], "spl_set_id": ["71224928-685a-355c-e053-2995a90a0a5b"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68071-4494-2)", "package_ndc": "68071-4494-2", "marketing_start_date": "20180716"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-4494-3)", "package_ndc": "68071-4494-3", "marketing_start_date": "20180716"}, {"sample": false, "description": "56 TABLET, FILM COATED in 1 BOTTLE (68071-4494-5)", "package_ndc": "68071-4494-5", "marketing_start_date": "20180716"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68071-4494-6)", "package_ndc": "68071-4494-6", "marketing_start_date": "20180716"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (68071-4494-8)", "package_ndc": "68071-4494-8", "marketing_start_date": "20180716"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-4494-9)", "package_ndc": "68071-4494-9", "marketing_start_date": "20180716"}], "brand_name": "Sertraline Hydrochloride", "product_id": "68071-4494_1a8d9cca-7c68-1e64-e063-6294a90a74bd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68071-4494", "generic_name": "Sertraline Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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"}