Cpc Chondrocyte Preparation Suspension
NDC 87622-003
View dosage, usage, ingredients, routes, and UNII mappings.
Product Information
This code was recently added to the official NDC directory and the product has entered commercial distribution.
Cpc Chondrocyte Preparation (cd73, cd90, cd105, icam-1, hgf) is a UNAPPROVED DRUG OTHER-approved product labeled by Zhongke Zhongluan Biotechnology (guangdong) Co., Ltd.. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a suspension for topical administration. This product entry covers the primary NDC 87622-003 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
87622-003
Proprietary Name:
Cpc Chondrocyte Preparation
Non-Proprietary Name: [1]
Cd73, Cd90, Cd105, Icam-1, Hgf
Substance Name: [2]
5'-nucleotidase; Intercellular Adhesion Molecule 1; Endoglin; Thy-1 Membrane Glycoprotein; Human Hepatocyte Growth Factor
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:
Clinical Specifications
Dosage Form:
Suspension
- A liquid1 dosage form that contains solid particles dispersed in a liquid vehicle.
Administration Route(s): [4]
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Labeler & Regulatory Data
Labeler Name: [5]
Labeler Code:
87622
Product Label ID:
Marketing Category: [8]
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Marketing Timeline
Start Marketing Date: [9]
07-14-2026
Listing Expiration Date: [11]
12-31-2027
Exclude Flag: [12]
N
Code Structure Chart
Product Details
What is NDC 87622-003?
The NDC code 87622-003 is assigned by the FDA to the product Cpc Chondrocyte Preparation. It is commonly known by its generic name, cd73, cd90, cd105, icam-1, hgf. This pharmaceutical product is labeled by Zhongke Zhongluan Biotechnology (guangdong) Co., Ltd. and is currently categorized as listed product. The medication is a suspension administered via topical route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 87622-003-01. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.
What are the uses of this product?
Mix gently before use. Each vial contains 3 mL; apply topically to the target skin / local area in a thin layer until absorbed; use once daily; use as a single-use vial after opening.
What are Active Ingredients of this product?
An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
- 5'-NUCLEOTIDASE .9 mg/mL - A glycoprotein enzyme present in various organs and in many cells. The enzyme catalyzes the hydrolysis of a 5'-ribonucleotide to a ribonucleoside and orthophosphate in the presence of water. It is cation-dependent and exists in a membrane-bound and soluble form. EC 3.1.3.5.
- INTERCELLULAR ADHESION MOLECULE 1 .9 mg/mL - A cell-surface ligand involved in leukocyte adhesion and inflammation. Its production is induced by gamma-interferon and it is required for neutrophil migration into inflamed tissue.
- ENDOGLIN .5 mg/mL - A membrane glycoprotein and ANGIOGENESIS FACTOR that is expressed by cells of the VASCULAR ENDOTHELIUM; VASCULAR SMOOTH MUSCLE; and MONOCYTES. It functions as a co-receptor for TRANSFORMING GROWTH FACTOR BETA and modulates CELL ADHESION. Mutations in the endoglin gene are associated with cases of HEREDITARY HEMORRHAGIC TELANGIECTASIA.
- THY-1 MEMBRANE GLYCOPROTEIN .7 mg/mL
- HUMAN HEPATOCYTE GROWTH FACTOR .9 mg/mL
Which are the associated UNII Codes?
The UNII codes for the active ingredients in this product are:
- 5'-NUCLEOTIDASE (UNII: T8635M4C7O)
- 5'-NUCLEOTIDASE (UNII: T8635M4C7O) (Active Moiety)
- INTERCELLULAR ADHESION MOLECULE 1 (UNII: 602I13CWRT)
- INTERCELLULAR ADHESION MOLECULE 1 (UNII: 602I13CWRT) (Active Moiety)
- ENDOGLIN (UNII: 1Y8Q34P575)
- ENDOGLIN (UNII: 1Y8Q34P575) (Active Moiety)
- THY-1 MEMBRANE GLYCOPROTEIN (UNII: EAD36Y912K)
- THY-1 MEMBRANE GLYCOPROTEIN (UNII: EAD36Y912K) (Active Moiety)
- HUMAN HEPATOCYTE GROWTH FACTOR (UNII: BEI7G52Q8Z)
- HUMAN HEPATOCYTE GROWTH FACTOR (UNII: BEI7G52Q8Z) (Active Moiety)
Which are the Inactive Ingredients associated UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
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Product & Regulatory Definitions
What is the Non-Proprietary Name? The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
What is the Substance Name? An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
What kind of product is this? Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
What is the Marketing Category? Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
What is the Listing Expiration Date? This is the date when the listing record will expire if not updated or certified by the product labeler.
What is the NDC Exclude Flag? This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".
