indapamide

Generic: indapamide

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

Drug Facts

Product Profile

Brand Name indapamide
Generic Name indapamide
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

indapamide 2.5 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-7247
Product ID 68788-7247_ce2108f0-ba96-484e-9fa0-01b3757b4511
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074722
Listing Expiration 2026-12-31
Marketing Start 2018-08-20

Pharmacologic Class

Established (EPC)
thiazide-like diuretic [epc]
Physiologic Effect
increased diuresis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687887247
Hyphenated Format 68788-7247

Supplemental Identifiers

RxCUI
197816
UNII
F089I0511L
NUI
N0000175359 N0000175420

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 indapamide (source: ndc)
Generic Name indapamide (source: ndc)
Application Number ANDA074722 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (68788-7247-1)
  • 30 TABLET, FILM COATED in 1 BOTTLE (68788-7247-3)
  • 60 TABLET, FILM COATED in 1 BOTTLE (68788-7247-6)
  • 90 TABLET, FILM COATED in 1 BOTTLE (68788-7247-9)
source: ndc

Packages (4)

68788-7247-1 100 TABLET, FILM COATED in 1 BOTTLE (68788-7247-1) 68788-7247-3 30 TABLET, FILM COATED in 1 BOTTLE (68788-7247-3) 68788-7247-6 60 TABLET, FILM COATED in 1 BOTTLE (68788-7247-6) 68788-7247-9 90 TABLET, FILM COATED in 1 BOTTLE (68788-7247-9)

Ingredients (1)

indapamide (2.5 mg/1)

Linked Drug Pages (1)

Indapamide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ce2108f0-ba96-484e-9fa0-01b3757b4511", "openfda": {"nui": ["N0000175359", "N0000175420"], "unii": ["F089I0511L"], "rxcui": ["197816"], "spl_set_id": ["59cd3331-7afe-432a-8b50-39533fd5f392"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68788-7247-1)", "package_ndc": "68788-7247-1", "marketing_start_date": "20180820"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-7247-3)", "package_ndc": "68788-7247-3", "marketing_start_date": "20180820"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-7247-6)", "package_ndc": "68788-7247-6", "marketing_start_date": "20180820"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-7247-9)", "package_ndc": "68788-7247-9", "marketing_start_date": "20180820"}], "brand_name": "Indapamide", "product_id": "68788-7247_ce2108f0-ba96-484e-9fa0-01b3757b4511", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "68788-7247", "generic_name": "Indapamide", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Indapamide", "active_ingredients": [{"name": "INDAPAMIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA074722", "marketing_category": "ANDA", "marketing_start_date": "20180820", "listing_expiration_date": "20261231"}