NDC 0781-3447-95 Angiomax
Bivalirudin
NDC Package Code 0781-3447-95
The NDC Code 0781-3447-95 is assigned to a package of 10 vial, single-use in 1 carton > 1 injection in 1 vial, single-use of Angiomax, a human prescription drug labeled by Sandoz Inc. The product's dosage form is injection and is administered via intravenous form.
NDC Code Structure
- 0781 - Sandoz Inc
- 0781-3447 - Angiomax
- 0781-3447-95 - 10 VIAL, SINGLE-USE in 1 CARTON
- 0781-3447 - Angiomax
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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NDC HCPCS Crosswalk
This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.
NDC 0781-3447-95 HCPCS crosswalk information with package details and bill units information.
NDC Billing Code | HCPCS Code | HCPCS Code Desc. | Dosage | Package Size | Package Quantity | Billable Units | Billable Units / Pkg |
---|---|---|---|---|---|---|---|
00781344795 | J0583 | Bivalirudin | 1 MG | 1 | 10 | 250 | 2500 |
* Please review the disclaimer below.