aminocaproic acid

Generic: aminocaproic acid

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name aminocaproic acid
Generic Name aminocaproic acid
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

aminocaproic acid 500 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-739
Product ID 60687-739_468beb69-98e3-926e-e063-6294a90a9da1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209060
Marketing Start 2023-03-10
Marketing End 2026-11-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687739
Hyphenated Format 60687-739

Supplemental Identifiers

RxCUI
197351
UNII
U6F3787206
NUI
N0000175634 N0000175632

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 ANDA209060 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 CARTON (60687-739-25) / 1 TABLET in 1 BLISTER PACK (60687-739-95)
source: ndc

Packages (1)

60687-739-25 30 BLISTER PACK in 1 CARTON (60687-739-25) / 1 TABLET in 1 BLISTER PACK (60687-739-95)

Ingredients (1)

aminocaproic acid (500 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": "468beb69-98e3-926e-e063-6294a90a9da1", "openfda": {"nui": ["N0000175634", "N0000175632"], "unii": ["U6F3787206"], "rxcui": ["197351"], "spl_set_id": ["4c2612ab-86a4-4c54-a5c0-e837f755965f"], "pharm_class_pe": ["Decreased Fibrinolysis [PE]"], "pharm_class_epc": ["Antifibrinolytic Agent [EPC]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (60687-739-25)  / 1 TABLET in 1 BLISTER PACK (60687-739-95)", "package_ndc": "60687-739-25", "marketing_end_date": "20261130", "marketing_start_date": "20230310"}], "brand_name": "Aminocaproic Acid", "product_id": "60687-739_468beb69-98e3-926e-e063-6294a90a9da1", "dosage_form": "TABLET", "pharm_class": ["Antifibrinolytic Agent [EPC]", "Decreased Fibrinolysis [PE]"], "product_ndc": "60687-739", "generic_name": "Aminocaproic Acid", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aminocaproic Acid", "active_ingredients": [{"name": "AMINOCAPROIC ACID", "strength": "500 mg/1"}], "application_number": "ANDA209060", "marketing_category": "ANDA", "marketing_end_date": "20261130", "marketing_start_date": "20230310"}