Solu-Cortef (Hydrocortisone sodium succinate) NDC 0009-0005

Product information

Brand name (proprietary)

Solu-Cortef

Generic name (nonproprietary)

hydrocortisone sodium succinate

Active ingredients

Hydrocortisone sodium succinate — 1000 mg/8mL

Dosage form

Injection, Powder, For solution

Route

Intramuscular, Intravenous

Labeler

Pharmacia & Upjohn Company LLCNDC labeler code 0009

Product type

Prescription drug

Marketing category

NDA — New Drug ApplicationApplication NDA 009866

Marketing start

Apr 27, 1955

Listing expires

Dec 31, 2027

Other FDA classes

Corticosteroid Hormone Receptor Agonists (Mechanism)

Identifiers

Product ID 0009-0005_d14e74dc-0706-4e2b-915d-ea9b0260e247SPL ID d14e74dc-0706-4e2b-915d-ea9b0260e247

Pharmacologic class

Corticosteroid

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

N400009000501 followed by a unit qualifier and the quantity Copy

Package 00009-0005-01. 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 0009-0005

What is NDC 0009-0005?

0009-0005 is the product NDC for Solu-Cortef (hydrocortisone sodium succinate), Hydrocortisone sodium succinate 1000 mg/8mL injection, powder, for solution, listed with the FDA by Pharmacia & Upjohn Company LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Solu-Cortef (Hydrocortisone sodium succinate).

What is the active ingredient?

Hydrocortisone sodium succinate.

Who is the labeler?

Pharmacia & Upjohn Company LLC, NDC labeler code 0009. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Solu-Cortef?

8 other product NDCs are listed under this name. See all Solu-Cortef NDCs.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory. See Billing references above.

Related NDCs: other Solu-Cortef products

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

Other NDCs under NDA 009866

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