hetastarch in sodium chloride

Generic: hetastarch

Labeler: hospira, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hetastarch in sodium chloride
Generic Name hetastarch
Labeler hospira, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

hetastarch 6 g/100mL

Manufacturer
Hospira, Inc.

Identifiers & Regulatory

Product NDC 0409-7248
Product ID 0409-7248_158d473a-3f10-496b-a7bc-a585db641ede
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number BA740193
Listing Expiration 2026-12-31
Marketing Start 2005-02-28

Pharmacologic Class

Established (EPC)
plasma volume expander [epc]
Mechanism of Action
osmotic activity [moa]
Chemical Structure
starch [cs]
Physiologic Effect
increased intravascular volume [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04097248
Hyphenated Format 0409-7248

Supplemental Identifiers

RxCUI
310757
UNII
875Y4127EA
NUI
N0000184175 N0000009361 N0000010288 M0020435

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 hetastarch in sodium chloride (source: ndc)
Generic Name hetastarch (source: ndc)
Application Number BA740193 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 6 g/100mL
source: ndc
Packaging
  • 12 CONTAINER in 1 CASE (0409-7248-03) / 500 mL in 1 CONTAINER (0409-7248-13)
source: ndc

Packages (1)

0409-7248-03 12 CONTAINER in 1 CASE (0409-7248-03) / 500 mL in 1 CONTAINER (0409-7248-13)

Ingredients (1)

hetastarch (6 g/100mL)

Linked Drug Pages (1)

Hetastarch in Sodium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "158d473a-3f10-496b-a7bc-a585db641ede", "openfda": {"nui": ["N0000184175", "N0000009361", "N0000010288", "M0020435"], "unii": ["875Y4127EA"], "rxcui": ["310757"], "spl_set_id": ["d64f961a-3e1f-4b04-cf83-604474af2775"], "pharm_class_cs": ["Starch [CS]"], "pharm_class_pe": ["Increased Intravascular Volume [PE]"], "pharm_class_epc": ["Plasma Volume Expander [EPC]"], "pharm_class_moa": ["Osmotic Activity [MoA]"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 CONTAINER in 1 CASE (0409-7248-03)  / 500 mL in 1 CONTAINER (0409-7248-13)", "package_ndc": "0409-7248-03", "marketing_start_date": "20050228"}], "brand_name": "Hetastarch in Sodium Chloride", "product_id": "0409-7248_158d473a-3f10-496b-a7bc-a585db641ede", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Intravascular Volume [PE]", "Osmotic Activity [MoA]", "Plasma Volume Expander [EPC]", "Starch [CS]"], "product_ndc": "0409-7248", "generic_name": "HETASTARCH", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hetastarch in Sodium Chloride", "active_ingredients": [{"name": "HETASTARCH", "strength": "6 g/100mL"}], "application_number": "BA740193", "marketing_category": "ANDA", "marketing_start_date": "20050228", "listing_expiration_date": "20261231"}