What is NDC 70710-1907?

70710-1907 is the product NDC for Hydrocortisone sodium succinate, Hydrocortisone sodium succinate 100 mg/2mL injection, listed with the FDA by Zydus Pharmaceuticals USA Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Zydus Pharmaceuticals USA Inc., NDC labeler code 70710. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Hydrocortisone sodium succinate?

3 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Hydrocortisone sodium succinate NDC 70710-1907

NDC codes

FDA NDC Directory

Product NDC (as listed)70710-1907Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70710-1907Add 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 NDC	11-digit (billing)	Package	Copy
70710-1907-1	70710190701	1 VIAL in 1 CARTON (70710-1907-1) / 2 mL in 1 VIALMarketed from May 9, 2026

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): Hydrocortisone sodium succinate
Generic name (nonproprietary): hydrocortisone sodium succinate
Active ingredients: Hydrocortisone sodium succinate — 100 mg/2mL
Dosage form: Injection
Route: Intramuscular, Intravenous
Labeler: Zydus Pharmaceuticals USA Inc.NDC labeler code 70710
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217191
Marketing start: May 9, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 70710-1907_9e47e808-7310-4c61-ac62-595a5c357123SPL ID 9e47e808-7310-4c61-ac62-595a5c357123SPL set ID 37534164-9de5-4bb3-9f87-341dfcf90883RxCUI 238755UNII 50LQB69S1Z
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

N470710190701 followed by a unit qualifier and the quantity

Package 70710-1907-01. 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

Current FDA label (SPL), effective May 8, 2026.

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 hydrocortisone sodium succinate for injection 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 (St…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70710-1907

What is NDC 70710-1907?: 70710-1907 is the product NDC for Hydrocortisone sodium succinate, Hydrocortisone sodium succinate 100 mg/2mL injection, listed with the FDA by Zydus Pharmaceuticals USA Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Hydrocortisone sodium succinate.
What is the active ingredient?: Hydrocortisone sodium succinate.
Who is the labeler?: Zydus Pharmaceuticals USA Inc., NDC labeler code 70710. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Hydrocortisone sodium succinate?: 3 other product NDCs are listed under this name. See all Hydrocortisone sodium succinate 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 Hydrocortisone sodium succinate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Hydrocortisone sodium succinate	Hydrocortisone sodium succinate 100 mg/2mL	Injection, Powder, For solutionIntramuscular, Intravenous	Apotex Corp.	60505-6411	60505-6411-00
Hydrocortisone sodium succinate	Hydrocortisone sodium succinate 100 mg/2mL	InjectionIntramuscular, Intravenous	Zydus Lifesciences Limited	70771-1966	70771-1966-01
Hydrocortisone sodium succinate	Hydrocortisone sodium succinate 100 mg/2mL	InjectionIntramuscular, Intravenous	Cipla USA Inc.	69097-004	69097-0004-67

Other NDCs under ANDA 217191

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

FDA NDC Directory listings under ANDA 217191
Product	Strength	Form · route	Labeler	Product NDC
Hydrocortisone sodium succinate	Hydrocortisone sodium succinate 100 mg/2mL	InjectionIntramuscular, Intravenous	Zydus Lifesciences Limited	70771-1966