bivalirudin

Generic: bivalirudin

Labeler: hainan shuangcheng pharmaceuticals co., ltd.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bivalirudin
Generic Name bivalirudin
Labeler hainan shuangcheng pharmaceuticals co., ltd.
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

bivalirudin 250 mg/1

Manufacturer
Hainan Shuangcheng Pharmaceuticals Co., Ltd.

Identifiers & Regulatory

Product NDC 52958-034
Product ID 52958-034_463422b6-e6d2-4319-a95e-aed834c2c844
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210031
Listing Expiration 2026-12-31
Marketing Start 2019-10-23

Pharmacologic Class

Established (EPC)
anti-coagulant [epc] direct thrombin inhibitor [epc]
Mechanism of Action
thrombin inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 52958034
Hyphenated Format 52958-034

Supplemental Identifiers

RxCUI
308769
UPC
0352958034010
UNII
TN9BEX005G
NUI
N0000175980 N0000175518 N0000009963

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 bivalirudin (source: ndc)
Generic Name bivalirudin (source: ndc)
Application Number ANDA210031 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 10 VIAL, SINGLE-USE in 1 CARTON (52958-034-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE
source: ndc

Packages (1)

52958-034-01 10 VIAL, SINGLE-USE in 1 CARTON (52958-034-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE

Ingredients (1)

bivalirudin (250 mg/1)

Linked Drug Pages (1)

Bivalirudin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "463422b6-e6d2-4319-a95e-aed834c2c844", "openfda": {"nui": ["N0000175980", "N0000175518", "N0000009963"], "upc": ["0352958034010"], "unii": ["TN9BEX005G"], "rxcui": ["308769"], "spl_set_id": ["61de12ff-e280-4bab-9804-43869ec45fa7"], "pharm_class_epc": ["Anti-coagulant [EPC]", "Direct Thrombin Inhibitor [EPC]"], "pharm_class_moa": ["Thrombin Inhibitors [MoA]"], "manufacturer_name": ["Hainan Shuangcheng Pharmaceuticals Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (52958-034-01)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE", "package_ndc": "52958-034-01", "marketing_start_date": "20191023"}], "brand_name": "Bivalirudin", "product_id": "52958-034_463422b6-e6d2-4319-a95e-aed834c2c844", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Direct Thrombin Inhibitor [EPC]", "Thrombin Inhibitors [MoA]"], "product_ndc": "52958-034", "generic_name": "Bivalirudin", "labeler_name": "Hainan Shuangcheng Pharmaceuticals Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bivalirudin", "active_ingredients": [{"name": "BIVALIRUDIN", "strength": "250 mg/1"}], "application_number": "ANDA210031", "marketing_category": "ANDA", "marketing_start_date": "20191023", "listing_expiration_date": "20261231"}