NDC codes

FDA NDC Directory
Product NDC (as listed)13533-692Labeler and product segments. Claims need a package NDC.
Product NDC at billing width13533-0692Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
13533-692-1613533069216135330692161 VIAL in 1 CARTON (13533-692-16) / 20 mL in 1 VIAL (13533-692-17)Marketed from Sep 26, 1994
13533-692-2013533069220135330692201 VIAL in 1 CARTON (13533-692-20) / 50 mL in 1 VIAL (13533-692-21)Marketed from Sep 26, 1994
13533-692-7113533069271135330692711 VIAL in 1 CARTON (13533-692-71) / 100 mL in 1 VIAL (13533-692-72)Marketed from Sep 26, 1994

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Plasbumin
Generic name (nonproprietary)
albumin (human)
Active ingredients
Albumin human — 5 g/20mL
Dosage form
Solution
Route
Intravenous
Labeler
GRIFOLS USA, LLCNDC labeler code 13533
Product type
Plasma derivative
Marketing category
BLA — Biologics License ApplicationApplication BLA 101138
Marketing start
Listing expires
Other FDA classes
Increased Intravascular Volume (Physiologic effect)Increased Oncotic Pressure (Physiologic effect)Osmotic Activity (Mechanism)Serum Albumin (Chemical/Ingredient)
Identifiers
Product ID 13533-692_38864ce1-9eaf-4d04-bfca-39205b0f1504SPL ID 38864ce1-9eaf-4d04-bfca-39205b0f1504
Pharmacologic class
Human Serum Albumin

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N413533069216 followed by a unit qualifier and the quantity

Package 13533-0692-16. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

The FDA listing for this product does not reference a label (SPL) set.

About NDC 13533-692

What is NDC 13533-692?
13533-692 is the product NDC for Plasbumin (albumin (human)), Albumin human 5 g/20mL solution, listed with the FDA by GRIFOLS USA, LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Plasbumin (Albumin (Human)).
What is the active ingredient?
Albumin human.
Who is the labeler?
GRIFOLS USA, LLC, NDC labeler code 13533. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Plasbumin?
2 other product NDCs are listed under this name. See all Plasbumin NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Plasbumin NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Plasbuminalbumin (human)Albumin human 2.5 g/50mLSolutionIntravenousGRIFOLS USA, LLC13533-69013533-0690-2013533-0690-2513533-0690-27
Plasbuminalbumin (human)Albumin human 10 g/50mLSolutionIntravenousGRIFOLS USA, LLC13533-69113533-0691-2013533-0691-71

Other NDCs under BLA 101138

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under BLA 101138
ProductStrengthForm · routeLabelerProduct NDC
Albukedalbumin (human)Albumin human 2.5 g/50mLSolutionIntravenousKEDRION BIOPHARMA, INC.76125-790
Albukedalbumin (human)Albumin human 10 g/50mLSolutionIntravenousKEDRION BIOPHARMA, INC.76125-791
Albukedalbumin (human)Albumin human 5 g/20mLSolutionIntravenousKEDRION BIOPHARMA, INC.76125-792
Plasbuminalbumin (human)Albumin human 2.5 g/50mLSolutionIntravenousGRIFOLS USA, LLC13533-690
Plasbuminalbumin (human)Albumin human 10 g/50mLSolutionIntravenousGRIFOLS USA, LLC13533-691

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