aminocaproic acid
Generic: aminocaproic acid
Labeler: amneal pharmaceuticals ny llcDrug Facts
Product Profile
Brand Name
aminocaproic acid
Generic Name
aminocaproic acid
Labeler
amneal pharmaceuticals ny llc
Dosage Form
TABLET
Routes
Active Ingredients
aminocaproic acid 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69238-1637
Product ID
69238-1637_6091bbf2-e45e-416d-bd4e-fc95dfeb609a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA212492
Listing Expiration
2026-12-31
Marketing Start
2019-11-30
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
692381637
Hyphenated Format
69238-1637
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
ANDA212492 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 30 TABLET in 1 BOTTLE, PLASTIC (69238-1637-3)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6091bbf2-e45e-416d-bd4e-fc95dfeb609a", "openfda": {"nui": ["N0000175634", "N0000175632"], "unii": ["U6F3787206"], "rxcui": ["197351"], "spl_set_id": ["4a22e559-2dac-42d7-af8d-eb0ebbc2f76d"], "pharm_class_pe": ["Decreased Fibrinolysis [PE]"], "pharm_class_epc": ["Antifibrinolytic Agent [EPC]"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (69238-1637-3)", "package_ndc": "69238-1637-3", "marketing_start_date": "20191130"}], "brand_name": "Aminocaproic acid", "product_id": "69238-1637_6091bbf2-e45e-416d-bd4e-fc95dfeb609a", "dosage_form": "TABLET", "pharm_class": ["Antifibrinolytic Agent [EPC]", "Decreased Fibrinolysis [PE]"], "product_ndc": "69238-1637", "generic_name": "Aminocaproic acid", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aminocaproic acid", "active_ingredients": [{"name": "AMINOCAPROIC ACID", "strength": "500 mg/1"}], "application_number": "ANDA212492", "marketing_category": "ANDA", "marketing_start_date": "20191130", "listing_expiration_date": "20261231"}