captopril

Generic: captopril

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name captopril
Generic Name captopril
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

captopril 25 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 55289-344
Product ID 55289-344_30c7bba4-3080-305f-e063-6394a90aea6e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074505
Listing Expiration 2026-12-31
Marketing Start 1996-02-13

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 55289344
Hyphenated Format 55289-344

Supplemental Identifiers

RxCUI
317173
UPC
0355289344308
UNII
9G64RSX1XD
NUI
N0000175562 N0000000181

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 ANDA074505 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (55289-344-30)
  • 90 TABLET in 1 BOTTLE, PLASTIC (55289-344-90)
source: ndc

Packages (2)

Ingredients (1)

captopril (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "30c7bba4-3080-305f-e063-6394a90aea6e", "openfda": {"nui": ["N0000175562", "N0000000181"], "upc": ["0355289344308"], "unii": ["9G64RSX1XD"], "rxcui": ["317173"], "spl_set_id": ["65ed6e70-f1ee-437e-965c-d1b1fdadd832"], "pharm_class_epc": ["Angiotensin Converting Enzyme Inhibitor [EPC]"], "pharm_class_moa": ["Angiotensin-converting Enzyme Inhibitors [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (55289-344-30)", "package_ndc": "55289-344-30", "marketing_start_date": "20110802"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (55289-344-90)", "package_ndc": "55289-344-90", "marketing_start_date": "20110802"}], "brand_name": "Captopril", "product_id": "55289-344_30c7bba4-3080-305f-e063-6394a90aea6e", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "55289-344", "generic_name": "Captopril", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Captopril", "active_ingredients": [{"name": "CAPTOPRIL", "strength": "25 mg/1"}], "application_number": "ANDA074505", "marketing_category": "ANDA", "marketing_start_date": "19960213", "listing_expiration_date": "20261231"}