aminocaproic acid

Generic: aminocaproic acid

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

Drug Facts

Product Profile

Brand Name aminocaproic acid
Generic Name aminocaproic acid
Labeler carnegie pharmaceuticals, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

aminocaproic acid 1000 mg/1

Manufacturer
Carnegie Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 80005-129
Product ID 80005-129_98b3715d-7fcf-4802-8b34-c1296b03b5fb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213928
Listing Expiration 2026-12-31
Marketing Start 2021-03-15

Pharmacologic Class

Established (EPC)
antifibrinolytic agent [epc]
Physiologic Effect
decreased fibrinolysis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 80005129
Hyphenated Format 80005-129

Supplemental Identifiers

RxCUI
197351 476271
UPC
0380005128085
UNII
U6F3787206
NUI
N0000175634 N0000175632

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 aminocaproic acid (source: ndc)
Generic Name aminocaproic acid (source: ndc)
Application Number ANDA213928 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (80005-129-08)
source: ndc

Packages (1)

80005-129-08 30 TABLET in 1 BOTTLE (80005-129-08)

Ingredients (1)

aminocaproic acid (1000 mg/1)

Linked Drug Pages (1)

AMINOCAPROIC ACID ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "98b3715d-7fcf-4802-8b34-c1296b03b5fb", "openfda": {"nui": ["N0000175634", "N0000175632"], "upc": ["0380005128085"], "unii": ["U6F3787206"], "rxcui": ["197351", "476271"], "spl_set_id": ["871ec401-30f8-4154-a16e-b82dc1e04b49"], "pharm_class_pe": ["Decreased Fibrinolysis [PE]"], "pharm_class_epc": ["Antifibrinolytic Agent [EPC]"], "manufacturer_name": ["Carnegie Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (80005-129-08)", "package_ndc": "80005-129-08", "marketing_start_date": "20210315"}], "brand_name": "AMINOCAPROIC ACID", "product_id": "80005-129_98b3715d-7fcf-4802-8b34-c1296b03b5fb", "dosage_form": "TABLET", "pharm_class": ["Antifibrinolytic Agent [EPC]", "Decreased Fibrinolysis [PE]"], "product_ndc": "80005-129", "generic_name": "AMINOCAPROIC ACID", "labeler_name": "Carnegie Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMINOCAPROIC ACID", "active_ingredients": [{"name": "AMINOCAPROIC ACID", "strength": "1000 mg/1"}], "application_number": "ANDA213928", "marketing_category": "ANDA", "marketing_start_date": "20210315", "listing_expiration_date": "20261231"}