captopril

Generic: captopril

Labeler: method pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name captopril
Generic Name captopril
Labeler method pharmaceuticals llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

captopril 25 mg/1

Manufacturer
Method Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 58657-936
Product ID 58657-936_457502be-feb2-5e2f-e063-6394a90aec0b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074677
Listing Expiration 2026-12-31
Marketing Start 2025-12-01

Pharmacologic Class

Established (EPC)
angiotensin converting enzyme inhibitor [epc]
Mechanism of Action
angiotensin-converting enzyme inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 58657936
Hyphenated Format 58657-936

Supplemental Identifiers

RxCUI
308962 308963 308964 317173
UPC
0358657738013 0358657735104 0358657737016 0358657735012 0358657738501 0358657736101 0358657736019 0358657737108
UNII
9G64RSX1XD
NUI
N0000175562 N0000000181

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 captopril (source: ndc)
Generic Name captopril (source: ndc)
Application Number ANDA074677 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (58657-936-01) / 1 TABLET in 1 BLISTER PACK (58657-936-10)
  • 30 BLISTER PACK in 1 CARTON (58657-936-03) / 1 TABLET in 1 BLISTER PACK (58657-936-10)
source: ndc

Packages (2)

58657-936-01 100 BLISTER PACK in 1 CARTON (58657-936-01) / 1 TABLET in 1 BLISTER PACK (58657-936-10) 58657-936-03 30 BLISTER PACK in 1 CARTON (58657-936-03) / 1 TABLET in 1 BLISTER PACK (58657-936-10)

Ingredients (1)

captopril (25 mg/1)

Linked Drug Pages (1)

captopril ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "457502be-feb2-5e2f-e063-6394a90aec0b", "openfda": {"nui": ["N0000175562", "N0000000181"], "upc": ["0358657738013", "0358657735104", "0358657737016", "0358657735012", "0358657738501", "0358657736101", "0358657736019", "0358657737108"], "unii": ["9G64RSX1XD"], "rxcui": ["308962", "308963", "308964", "317173"], "spl_set_id": ["1a91ac7f-b75d-d111-e063-6394a90a2a93"], "pharm_class_epc": ["Angiotensin Converting Enzyme Inhibitor [EPC]"], "pharm_class_moa": ["Angiotensin-converting Enzyme Inhibitors [MoA]"], "manufacturer_name": ["Method Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (58657-936-01)  / 1 TABLET in 1 BLISTER PACK (58657-936-10)", "package_ndc": "58657-936-01", "marketing_start_date": "20251201"}, {"sample": false, "description": "30 BLISTER PACK in 1 CARTON (58657-936-03)  / 1 TABLET in 1 BLISTER PACK (58657-936-10)", "package_ndc": "58657-936-03", "marketing_start_date": "20251201"}], "brand_name": "captopril", "product_id": "58657-936_457502be-feb2-5e2f-e063-6394a90aec0b", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "58657-936", "generic_name": "captopril", "labeler_name": "Method Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "captopril", "active_ingredients": [{"name": "CAPTOPRIL", "strength": "25 mg/1"}], "application_number": "ANDA074677", "marketing_category": "ANDA", "marketing_start_date": "20251201", "listing_expiration_date": "20261231"}