heparin sodium in sodium chloride

Generic: heparin sodium in sodium chloride

Labeler: b. braun medical inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name heparin sodium in sodium chloride
Generic Name heparin sodium in sodium chloride
Labeler b. braun medical inc.
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

heparin sodium 200 [USP'U]/100mL

Manufacturer
B. Braun Medical Inc.

Identifiers & Regulatory

Product NDC 0264-9872
Product ID 0264-9872_48e17807-e73d-4ea2-81bc-901355903aa7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019953
Listing Expiration 2026-12-31
Marketing Start 1992-07-20

Pharmacologic Class

Classes
anti-coagulant [epc] heparin [cs] unfractionated heparin [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02649872
Hyphenated Format 0264-9872

Supplemental Identifiers

RxCUI
1658690 1658692
UNII
ZZ45AB24CA

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 heparin sodium in sodium chloride (source: ndc)
Generic Name heparin sodium in sodium chloride (source: ndc)
Application Number NDA019953 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 200 [USP'U]/100mL
source: ndc
Packaging
  • 12 CONTAINER in 1 CASE (0264-9872-00) / 1000 mL in 1 CONTAINER
  • 24 CONTAINER in 1 CASE (0264-9872-10) / 500 mL in 1 CONTAINER
source: ndc

Packages (2)

0264-9872-00 12 CONTAINER in 1 CASE (0264-9872-00) / 1000 mL in 1 CONTAINER 0264-9872-10 24 CONTAINER in 1 CASE (0264-9872-10) / 500 mL in 1 CONTAINER

Ingredients (1)

heparin sodium (200 [USP'U]/100mL)

Linked Drug Pages (1)

Heparin Sodium in Sodium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "48e17807-e73d-4ea2-81bc-901355903aa7", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1658690", "1658692"], "spl_set_id": ["a3041c04-0ea8-4d36-81ce-c5091c906316"], "manufacturer_name": ["B. Braun Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 CONTAINER in 1 CASE (0264-9872-00)  / 1000 mL in 1 CONTAINER", "package_ndc": "0264-9872-00", "marketing_start_date": "20231215"}, {"sample": false, "description": "24 CONTAINER in 1 CASE (0264-9872-10)  / 500 mL in 1 CONTAINER", "package_ndc": "0264-9872-10", "marketing_start_date": "19920720"}], "brand_name": "Heparin Sodium in Sodium Chloride", "product_id": "0264-9872_48e17807-e73d-4ea2-81bc-901355903aa7", "dosage_form": "INJECTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "0264-9872", "generic_name": "Heparin Sodium in Sodium Chloride", "labeler_name": "B. Braun Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium in Sodium Chloride", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "200 [USP'U]/100mL"}], "application_number": "NDA019953", "marketing_category": "NDA", "marketing_start_date": "19920720", "listing_expiration_date": "20261231"}