irbesartan

Generic: irbesartan

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name irbesartan
Generic Name irbesartan
Labeler camber pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

irbesartan 150 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-730
Product ID 31722-730_088a5ed0-89a1-c72a-e063-6394a90a74af
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202910
Listing Expiration 2026-12-31
Marketing Start 2012-09-27

Pharmacologic Class

Established (EPC)
angiotensin 2 receptor blocker [epc]
Mechanism of Action
angiotensin 2 receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722730
Hyphenated Format 31722-730

Supplemental Identifiers

RxCUI
200094 200095 200096
UNII
J0E2756Z7N
NUI
N0000000070 N0000175561

Packaging Origin

Original Packager
true

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 ANDA202910 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 500 TABLET in 1 BOTTLE (31722-730-05)
  • 30 TABLET in 1 BOTTLE (31722-730-30)
  • 120 BLISTER PACK in 1 CARTON (31722-730-31) / 10 TABLET in 1 BLISTER PACK
  • 90 TABLET in 1 BOTTLE (31722-730-90)
source: ndc

Packages (4)

31722-730-05 500 TABLET in 1 BOTTLE (31722-730-05) 31722-730-30 30 TABLET in 1 BOTTLE (31722-730-30) 31722-730-31 120 BLISTER PACK in 1 CARTON (31722-730-31) / 10 TABLET in 1 BLISTER PACK 31722-730-90 90 TABLET in 1 BOTTLE (31722-730-90)

Ingredients (1)

irbesartan (150 mg/1)

Linked Drug Pages (1)

Irbesartan ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "088a5ed0-89a1-c72a-e063-6394a90a74af", "openfda": {"nui": ["N0000000070", "N0000175561"], "unii": ["J0E2756Z7N"], "rxcui": ["200094", "200095", "200096"], "spl_set_id": ["33416f1e-adee-4a45-b6fe-1fc39044e307"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (31722-730-05)", "package_ndc": "31722-730-05", "marketing_start_date": "20120927"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (31722-730-30)", "package_ndc": "31722-730-30", "marketing_start_date": "20120927"}, {"sample": false, "description": "120 BLISTER PACK in 1 CARTON (31722-730-31)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "31722-730-31", "marketing_start_date": "20120927"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (31722-730-90)", "package_ndc": "31722-730-90", "marketing_start_date": "20120927"}], "brand_name": "Irbesartan", "product_id": "31722-730_088a5ed0-89a1-c72a-e063-6394a90a74af", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "31722-730", "generic_name": "Irbesartan", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Irbesartan", "active_ingredients": [{"name": "IRBESARTAN", "strength": "150 mg/1"}], "application_number": "ANDA202910", "marketing_category": "ANDA", "marketing_start_date": "20120927", "listing_expiration_date": "20261231"}