exemestane
Generic: exemestane
Labeler: zydus lifesciences limitedDrug Facts
Product Profile
Brand Name
exemestane
Generic Name
exemestane
Labeler
zydus lifesciences limited
Dosage Form
TABLET
Routes
Active Ingredients
exemestane 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70771-1374
Product ID
70771-1374_7892e262-ddad-4e1d-909d-d8590bb082de
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202602
Listing Expiration
2026-12-31
Marketing Start
2018-10-08
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
707711374
Hyphenated Format
70771-1374
Supplemental Identifiers
RxCUI
UNII
NUI
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
exemestane (source: ndc)
Generic Name
exemestane (source: ndc)
Application Number
ANDA202602 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (70771-1374-3)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7892e262-ddad-4e1d-909d-d8590bb082de", "openfda": {"nui": ["N0000175563", "N0000175080"], "unii": ["NY22HMQ4BX"], "rxcui": ["310261"], "spl_set_id": ["fab5468a-d5b7-45e3-b8b2-ed902fddd3a6"], "pharm_class_epc": ["Aromatase Inhibitor [EPC]"], "pharm_class_moa": ["Aromatase Inhibitors [MoA]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (70771-1374-3)", "package_ndc": "70771-1374-3", "marketing_start_date": "20181008"}], "brand_name": "Exemestane", "product_id": "70771-1374_7892e262-ddad-4e1d-909d-d8590bb082de", "dosage_form": "TABLET", "pharm_class": ["Aromatase Inhibitor [EPC]", "Aromatase Inhibitors [MoA]"], "product_ndc": "70771-1374", "generic_name": "Exemestane", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Exemestane", "active_ingredients": [{"name": "EXEMESTANE", "strength": "25 mg/1"}], "application_number": "ANDA202602", "marketing_category": "ANDA", "marketing_start_date": "20181008", "listing_expiration_date": "20261231"}