NDC codes

FDA NDC Directory
Product NDC (as listed)70436-225Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70436-0225Add 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
70436-225-4770436022547704360225471 BLISTER PACK in 1 CARTON (70436-225-47) / 10 CAPSULE in 1 BLISTER PACKMarketed from Jan 1, 2024

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
oseltamivir phosphate
Generic name (nonproprietary)
oseltamivir phosphate
Active ingredients
Oseltamivir phosphate — 75 mg/1
Dosage form
Capsule
Route
Oral
Labeler
Slate Run Pharmaceuticals, LLCNDC labeler code 70436
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 218009
Marketing start
Listing expires
Other FDA classes
Neuraminidase Inhibitors (Mechanism)
Identifiers
Product ID 70436-225_32f5c180-8169-55c5-e063-6294a90a3f20SPL ID 32f5c180-8169-55c5-e063-6294a90a3f20SPL set ID 613c8c4d-e647-4a4b-ac9b-c39aaa781aceRxCUI 312122UNII 4A3O49NGEZUPC 0370436225477
Pharmacologic class
Neuraminidase Inhibitor

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 HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N470436022547 followed by a unit qualifier and the quantity

Package 70436-0225-47. 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)

Oseltamivir phosphate is an influenza neuraminidase inhibitor (NAI) indicated for: Treatment of acute, uncomplicated influenza A and B in patients 2 weeks of age and older who have been symptomatic for no more than 48 hours. ( 1.1 ) Prophylaxis of influenza A and B in patients 1 year and older. ( 1.2 ) Limitations of Use: Not a substitute for annual influenza vaccination. ( 1.3 ) Consider available information on influenza drug susceptibility patterns and treatment effects when deciding whether to use. ( 1.3 ) Not recommended for patients with end-stage renal disease not undergoing dialysis. ( 1.3 ) 1.1 Treatment of Influenza Oseltamivir phosphate is indicated for the treatment of acute, unc…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70436-225

What is NDC 70436-225?
70436-225 is the product NDC for oseltamivir phosphate, Oseltamivir phosphate 75 mg/1 capsule, listed with the FDA by Slate Run Pharmaceuticals, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
oseltamivir phosphate.
What is the active ingredient?
Oseltamivir phosphate.
Who is the labeler?
Slate Run Pharmaceuticals, LLC, NDC labeler code 70436. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for oseltamivir phosphate?
107 other product NDCs are listed under this name. See all oseltamivir phosphate 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 oseltamivir phosphate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Oseltamivir PhosphateOseltamivir phosphate 75 mg/1CapsuleOralREMEDYREPACK INC.70518-477070518-4770-00
Oseltamivir PhosphateOseltamivir phosphate 6 mg/mLFor suspensionOralAlembic Pharmaceuticals Limited46708-76946708-0769-60
Oseltamivir PhosphateOseltamivir phosphate 6 mg/mLFor suspensionOralAlembic Pharmaceuticals Inc.62332-76962332-0769-60
Oseltamivir PhosphateOseltamivir phosphate 6 mg/mLSuspensionOralHEC Pharm USA Inc.72303-085172303-0851-01
Oseltamivir PhosphateOseltamivir phosphate 75 mg/1CapsuleOralPreferred Pharmaceuticals Inc.68788-406668788-4066-01
oseltamivir phosphateOseltamivir phosphate 30 mg/1CapsuleOralZhejiang Poly Pharm. Co., Ltd.72673-10172673-0101-10
oseltamivir phosphateOseltamivir phosphate 45 mg/1CapsuleOralZhejiang Poly Pharm. Co., Ltd.72673-10272673-0102-10
Oseltamivir phosphateOseltamivir phosphate 45 mg/1CapsuleOralShandong New Time Pharmaceutical Co., Ltd.42677-32142677-0321-01
Oseltamivir phosphateOseltamivir phosphate 30 mg/1CapsuleOralShandong New Time Pharmaceutical Co., Ltd.42677-32042677-0320-01
Oseltamivir phosphateOseltamivir phosphate 75 mg/1CapsuleOralShandong New Time Pharmaceutical Co., Ltd.42677-32242677-0322-01

All 108 oseltamivir phosphate NDCs

Other NDCs under ANDA 218009

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

FDA NDC Directory listings under ANDA 218009
ProductStrengthForm · routeLabelerProduct NDC
oseltamivir phosphateOseltamivir phosphate 30 mg/1CapsuleOralZhejiang Poly Pharm. Co., Ltd.72673-101
oseltamivir phosphateOseltamivir phosphate 45 mg/1CapsuleOralZhejiang Poly Pharm. Co., Ltd.72673-102
oseltamivir phosphateOseltamivir phosphate 75 mg/1CapsuleOralZhejiang Poly Pharm. Co., Ltd.72673-103

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