irbesartan
Generic: irbesartan
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
irbesartan
Generic Name
irbesartan
Labeler
remedyrepack inc.
Dosage Form
TABLET
Routes
Active Ingredients
irbesartan 150 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-1690
Product ID
70518-1690_4961546d-44ed-5dab-e063-6394a90a3cde
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203071
Listing Expiration
2027-12-31
Marketing Start
2018-11-23
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705181690
Hyphenated Format
70518-1690
Supplemental Identifiers
RxCUI
UNII
NUI
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
irbesartan (source: ndc)
Generic Name
irbesartan (source: ndc)
Application Number
ANDA203071 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 150 mg/1
Packaging
- 90 TABLET in 1 BOTTLE, PLASTIC (70518-1690-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4961546d-44ed-5dab-e063-6394a90a3cde", "openfda": {"nui": ["N0000000070", "N0000175561"], "unii": ["J0E2756Z7N"], "rxcui": ["200095"], "spl_set_id": ["029a90b6-0722-49be-8400-3ec29526aafd"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-1690-1)", "package_ndc": "70518-1690-1", "marketing_start_date": "20230419"}], "brand_name": "Irbesartan", "product_id": "70518-1690_4961546d-44ed-5dab-e063-6394a90a3cde", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "70518-1690", "generic_name": "Irbesartan", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Irbesartan", "active_ingredients": [{"name": "IRBESARTAN", "strength": "150 mg/1"}], "application_number": "ANDA203071", "marketing_category": "ANDA", "marketing_start_date": "20181123", "listing_expiration_date": "20271231"}