NDC codes

FDA NDC Directory
Product NDC (as listed)55154-3942Labeler and product segments. Claims need a package NDC.
Product NDC at billing width55154-3942Add 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
55154-3942-555154394205551543942055 VIAL, SINGLE-DOSE in 1 BAG (55154-3942-5) / 2 mL in 1 VIAL, SINGLE-DOSEMarketed from Apr 27, 1955

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
Solu-Cortef
Generic name (nonproprietary)
hydrocortisone sodium succinate
Active ingredients
Hydrocortisone sodium succinate — 100 mg/2mL
Dosage form
Injection, Powder, For solution
Route
Intramuscular, Intravenous
Labeler
Cardinal Health 107, LLCNDC labeler code 55154
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 009866
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 55154-3942_bc348e8f-69c8-4cf4-a685-324ee3ebde87SPL ID bc348e8f-69c8-4cf4-a685-324ee3ebde87SPL set ID f5bb0854-a477-4e59-914b-eeeaef92a596RxCUI 105398, 238755UNII 50LQB69S1ZUPC 0055154394253
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

N455154394205 followed by a unit qualifier and the quantity

Package 55154-3942-05. 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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

INDICATIONS AND USAGE When oral therapy is not feasible, and the strength, dosage form, and route of administration of the drug reasonably lend the preparation to the treatment of the condition, the intravenous or intramuscular use of SOLU-CORTEF Sterile Powder is indicated as follows: Allergic states: Control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, serum sickness, transfusion reactions. Dermatologic diseases: Bullous dermatitis herpetiformis, exfoliative erythroderma, mycosis fungoides, pemphigus, severe erythema multiforme (Stevens-Johnson synd…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 55154-3942

What is NDC 55154-3942?
55154-3942 is the product NDC for Solu-Cortef (hydrocortisone sodium succinate), Hydrocortisone sodium succinate 100 mg/2mL injection, powder, for solution, listed with the FDA by Cardinal Health 107, 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?
Cardinal Health 107, LLC, NDC labeler code 55154. 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.

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

Other Solu-Cortef NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Solu-CortefHydrocortisone sodium succinate 100 mg/2mLInjection, Powder, For solutionIntramuscular, IntravenousHF Acquisition Co. LLC, DBA HealthFirst51662-126151662-1261-0151662-1261-03
Solu-CortefHydrocortisone sodium succinate 250 mg/2mLInjection, Powder, For solutionIntramuscular, IntravenousHF Acquisition Co. LLC, DBA HealthFirst51662-126251662-1262-01
Solu-Cortefhydrocortisone sodium succinateHydrocortisone sodium succinate 1000 mg/8mLInjection, Powder, For solutionIntramuscular, IntravenousPharmacia & Upjohn Company LLC0009-000500009-0005-01
Solu-Cortefhydrocortisone sodium succinateHydrocortisone sodium succinate 100 mg/2mLInjection, Powder, For solutionIntramuscular, IntravenousPharmacia & Upjohn Company LLC0009-001100009-0011-0300009-0011-04
Solu-Cortefhydrocortisone sodium succinateHydrocortisone sodium succinate 250 mg/2mLInjection, Powder, For solutionIntramuscular, IntravenousPharmacia & Upjohn Company LLC0009-001300009-0013-0500009-0013-06
Solu-Cortefhydrocortisone sodium succinateHydrocortisone sodium succinate 500 mg/4mLInjection, Powder, For solutionIntramuscular, IntravenousPharmacia & Upjohn Company LLC0009-001600009-0016-12
Solu-Cortefhydrocortisone sodium succinateHydrocortisone sodium succinate 100 mg/2mLInjection, Powder, For solutionIntramuscular, IntravenousPharmacia & Upjohn Company LLC0009-082500009-0825-01
Solu-Cortefhydrocortisone sodium succinateHydrocortisone sodium succinate 100 mg/2mLInjection, Powder, For solutionIntramuscular, IntravenousProPharma Distribution84549-01184549-0011-04

Other NDCs under NDA 009866

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

FDA NDC Directory listings under NDA 009866
ProductStrengthForm · routeLabelerProduct NDC
Solu-Cortefhydrocortisone sodium succinateHydrocortisone sodium succinate 1000 mg/8mLInjection, Powder, For solutionIntramuscular, IntravenousPharmacia & Upjohn Company LLC0009-0005
Solu-Cortefhydrocortisone sodium succinateHydrocortisone sodium succinate 100 mg/2mLInjection, Powder, For solutionIntramuscular, IntravenousPharmacia & Upjohn Company LLC0009-0011
Solu-Cortefhydrocortisone sodium succinateHydrocortisone sodium succinate 250 mg/2mLInjection, Powder, For solutionIntramuscular, IntravenousPharmacia & Upjohn Company LLC0009-0013
Solu-Cortefhydrocortisone sodium succinateHydrocortisone sodium succinate 500 mg/4mLInjection, Powder, For solutionIntramuscular, IntravenousPharmacia & Upjohn Company LLC0009-0016
Solu-Cortefhydrocortisone sodium succinateHydrocortisone sodium succinate 100 mg/2mLInjection, Powder, For solutionIntramuscular, IntravenousPharmacia & Upjohn Company LLC0009-0825
Solu-CortefHydrocortisone sodium succinate 100 mg/2mLInjection, Powder, For solutionIntramuscular, IntravenousHF Acquisition Co. LLC, DBA HealthFirst51662-1261
Solu-CortefHydrocortisone sodium succinate 250 mg/2mLInjection, Powder, For solutionIntramuscular, IntravenousHF Acquisition Co. LLC, DBA HealthFirst51662-1262
Solu-Cortefhydrocortisone sodium succinateHydrocortisone sodium succinate 100 mg/2mLInjection, Powder, For solutionIntramuscular, IntravenousProPharma Distribution84549-011

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