Drug
Plasmanate NDC Codes
Plasmanate is listed in the FDA NDC Directory as 1 finished product from 1 labeler.
Overview
Active ingredient: Albumin human. Each product below links to its own NDC page with package NDCs in 10- and 11-digit form.
- Generic name
- Plasma Protein Fraction (Human)
- Active ingredients
- Albumin human
- Labelers
- GRIFOLS USA, LLC
- Strengths
- Albumin human 2.5 g/50mL
- Dosage forms
- Solution
- Routes
- Intravenous
- Drug classes (FDA established)
- Human Serum Albumin
- HCPCS / J-code
- None in Med-Code's directory for these products
- Package NDCs
- 1
NDC codes
Newest listings first. Each row links to the product’s NDC page.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) | HCPCS |
|---|---|---|---|---|---|---|
| Plasmanateplasma protein fraction (human) | Albumin human 2.5 g/50mL | SolutionIntravenous | GRIFOLS USA, LLC | 13533-613 | 13533-0613-25 | — |
Plasmanate: common questions
- What is the NDC for Plasmanate?
- Plasmanate has 1 product NDC, one for each strength, dosage form and labeler; each product NDC then has one package NDC per package size. Pick the row for your product above to see its package NDCs.
- Is there a J-code for Plasmanate?
- Med-Code's curated HCPCS directory has no drug-specific code for these products. Drugs dispensed by a pharmacy are billed by NDC. NDC vs J-code.
- Which NDC goes on a claim?
- The package NDC of what was given, in 11-digit form. How to convert a 10-digit NDC.