tranexamic acid

Generic: tranexamic acid

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

Drug Facts

Product Profile

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

tranexamic acid 650 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-750
Product ID 60687-750_4c258bec-ab80-cb54-e063-6394a90a1893
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203256
Listing Expiration 2027-12-31
Marketing Start 2023-10-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687750
Hyphenated Format 60687-750

Supplemental Identifiers

RxCUI
883826
UNII
6T84R30KC1
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 tranexamic acid (source: ndc)
Generic Name tranexamic acid (source: ndc)
Application Number ANDA203256 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 CARTON (60687-750-21) / 1 TABLET in 1 BLISTER PACK (60687-750-11)
source: ndc

Packages (1)

60687-750-21 30 BLISTER PACK in 1 CARTON (60687-750-21) / 1 TABLET in 1 BLISTER PACK (60687-750-11)

Ingredients (1)

tranexamic acid (650 mg/1)

Linked Drug Pages (1)

Tranexamic Acid ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4c258bec-ab80-cb54-e063-6394a90a1893", "openfda": {"nui": ["N0000175634", "N0000175632"], "unii": ["6T84R30KC1"], "rxcui": ["883826"], "spl_set_id": ["cbc6f5b3-927e-4a94-8836-dbcd47ef97a8"], "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 (60687-750-21)  / 1 TABLET in 1 BLISTER PACK (60687-750-11)", "package_ndc": "60687-750-21", "marketing_start_date": "20231001"}], "brand_name": "Tranexamic Acid", "product_id": "60687-750_4c258bec-ab80-cb54-e063-6394a90a1893", "dosage_form": "TABLET", "pharm_class": ["Antifibrinolytic Agent [EPC]", "Decreased Fibrinolysis [PE]"], "product_ndc": "60687-750", "generic_name": "Tranexamic Acid", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tranexamic Acid", "active_ingredients": [{"name": "TRANEXAMIC ACID", "strength": "650 mg/1"}], "application_number": "ANDA203256", "marketing_category": "ANDA", "marketing_start_date": "20231001", "listing_expiration_date": "20271231"}