acd a

Generic: dextrose monohydrate, sodium citrate, and citric acid monohydrate

Labeler: terumo bct ltd
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acd a
Generic Name dextrose monohydrate, sodium citrate, and citric acid monohydrate
Labeler terumo bct ltd
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

citric acid monohydrate .8 g/100mL, dextrose monohydrate 2.45 g/100mL, sodium citrate, unspecified form 2.2 g/100mL

Manufacturer
Terumo BCT Ltd

Identifiers & Regulatory

Product NDC 14537-967
Product ID 14537-967_b4f43833-2089-467d-bfd3-03817b19cab6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number BA010228
Listing Expiration 2026-12-31
Marketing Start 2002-02-25

Pharmacologic Class

Classes
acidifying activity [moa] anti-coagulant [epc] calcium chelating activity [moa] calculi dissolution agent [epc] decreased coagulation factor activity [pe] increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 14537967
Hyphenated Format 14537-967

Supplemental Identifiers

UNII
2968PHW8QP LX22YL083G 1Q73Q2JULR

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 acd a (source: ndc)
Generic Name dextrose monohydrate, sodium citrate, and citric acid monohydrate (source: ndc)
Application Number BA010228 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • .8 g/100mL
  • 2.45 g/100mL
  • 2.2 g/100mL
source: ndc
Packaging
  • 12 BAG in 1 CASE (14537-967-75) / 750 mL in 1 BAG
source: ndc

Packages (1)

Ingredients (3)

citric acid monohydrate (.8 g/100mL) dextrose monohydrate (2.45 g/100mL) sodium citrate, unspecified form (2.2 g/100mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "b4f43833-2089-467d-bfd3-03817b19cab6", "openfda": {"unii": ["2968PHW8QP", "LX22YL083G", "1Q73Q2JULR"], "spl_set_id": ["570770de-9b48-4fc1-a1ee-06002ca9504f"], "manufacturer_name": ["Terumo BCT Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 BAG in 1 CASE (14537-967-75)  / 750 mL in 1 BAG", "package_ndc": "14537-967-75", "marketing_start_date": "20020225"}], "brand_name": "ACD A", "product_id": "14537-967_b4f43833-2089-467d-bfd3-03817b19cab6", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "14537-967", "generic_name": "Dextrose Monohydrate, Sodium Citrate, and Citric Acid Monohydrate", "labeler_name": "Terumo BCT Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ACD", "brand_name_suffix": "A", "active_ingredients": [{"name": "CITRIC ACID MONOHYDRATE", "strength": ".8 g/100mL"}, {"name": "DEXTROSE MONOHYDRATE", "strength": "2.45 g/100mL"}, {"name": "SODIUM CITRATE, UNSPECIFIED FORM", "strength": "2.2 g/100mL"}], "application_number": "BA010228", "marketing_category": "ANDA", "marketing_start_date": "20020225", "listing_expiration_date": "20261231"}