sertraline hydrochloride
Generic: sertraline hydrochloride
Labeler: zydus lifesciences limitedDrug Facts
Product Profile
Brand Name
sertraline hydrochloride
Generic Name
sertraline hydrochloride
Labeler
zydus lifesciences limited
Dosage Form
CAPSULE
Routes
Active Ingredients
sertraline hydrochloride 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70771-1914
Product ID
70771-1914_e5ff2f30-1085-40b7-a090-a8393a7c422f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA220275
Listing Expiration
2027-12-31
Marketing Start
2026-01-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
707711914
Hyphenated Format
70771-1914
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
ANDA220275 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE (70771-1914-3)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e5ff2f30-1085-40b7-a090-a8393a7c422f", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["251201", "410584"], "spl_set_id": ["96dedceb-81ad-447c-800e-800cf473d4e4"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (70771-1914-3)", "package_ndc": "70771-1914-3", "marketing_start_date": "20260129"}], "brand_name": "Sertraline Hydrochloride", "product_id": "70771-1914_e5ff2f30-1085-40b7-a090-a8393a7c422f", "dosage_form": "CAPSULE", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70771-1914", "generic_name": "Sertraline Hydrochloride", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sertraline Hydrochloride", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA220275", "marketing_category": "ANDA", "marketing_start_date": "20260129", "listing_expiration_date": "20271231"}