What is NDC 70710-1014?

70710-1014 is the product NDC for Phytonadione, Phytonadione 5 mg/1 tablet, listed with the FDA by Zydus Pharmaceuticals USA Inc.. It has 3 package NDCs, 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 Phytonadione?

31 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Phytonadione NDC 70710-1014 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70710-1014Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70710-1014Add 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
70710-1014-1	70710101401	1 BOTTLE in 1 CARTON (70710-1014-1) / 100 TABLET in 1 BOTTLEMarketed from Feb 22, 2019 · Sample package
70710-1014-3	70710101403	30 TABLET in 1 BOTTLE (70710-1014-3)Marketed from Nov 1, 2021 · Sample package
70710-1014-4	70710101404	10 BLISTER PACK in 1 CARTON (70710-1014-4) / 10 TABLET in 1 BLISTER PACK (70710-1014-2)Marketed from Feb 22, 2019 · Sample package

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): Phytonadione
Generic name (nonproprietary): phytonadione
Active ingredients: Phytonadione — 5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Zydus Pharmaceuticals USA Inc.NDC labeler code 70710
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 210189
Marketing start: Feb 22, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Increased Prothrombin Activity (Physiologic effect)Reversed Anticoagulation Activity (Physiologic effect)Vitamin K (Chemical structure)
Identifiers: Product ID 70710-1014_e01282e9-c321-44ca-adc7-93d3e808fe4cSPL ID e01282e9-c321-44ca-adc7-93d3e808fe4cSPL set ID 6c992275-b040-42d0-9eff-570dce4272feRxCUI 198102UNII A034SE7857
Pharmacologic class: Vitamin K; Warfarin Reversal Agent

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

N470710101401 followed by a unit qualifier and the quantity

Package 70710-1014-01. 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 Aug 5, 2024.

Indications (excerpt from the label)

Phytonadione is indicated for the treatment of adults with the following coagulation disorders which are due to faulty formation of factors II, VII, IX and X when caused by vitamin K deficiency or interference with vitamin K activity. anticoagulant-induced hypoprothrombinemia caused by coumarin or indanedione derivatives; hypoprothrombinemia secondary to antibacterial therapy; hypoprothrombinemia secondary to factors limiting absorption or synthesis of vitamin K, e.g., obstructive jaundice, biliary fistula, sprue, ulcerative colitis, celiac disease, intestinal resection, cystic fibrosis of the pancrease, and regional enteritis; Other drug-induced hypoprothrombinemia where it is definitely sh…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70710-1014

What is NDC 70710-1014?: 70710-1014 is the product NDC for Phytonadione, Phytonadione 5 mg/1 tablet, listed with the FDA by Zydus Pharmaceuticals USA Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Phytonadione.
What is the active ingredient?: Phytonadione.
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 Phytonadione?: 31 other product NDCs are listed under this name. See all Phytonadione 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 Phytonadione NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Phytonadione	Phytonadione 5 mg/1	TabletOral	Safecor Health, LLC	48433-160	48433-0160-03
Phytonadione	Phytonadione 1 mg/.5mL	Injection, EmulsionIntramuscular, Intravenous, Subcutaneous	Sun Pharmaceutical Industries, Inc.	70095-154	70095-0154-02
Phytonadione	Phytonadione 10 mg/mL	Injection, EmulsionIntramuscular, Intravenous, Subcutaneous	Amneal Pharmaceuticals Private Limited	80830-1683	80830-1683-03
Phytonadione	Phytonadione 1 mg/.5mL	Injection, EmulsionIntramuscular, Intravenous, Subcutaneous	Orbicular Pharmaceutical Technologies Private Limited	81607-020	81607-0020-02
Phytonadione	Phytonadione 1 mg/.5mL	Injection, EmulsionIntramuscular, Intravenous, Subcutaneous	Baxter Healthcare Corporation	43066-132	43066-0132-10
Phytonadione	Phytonadione 1 mg/.5mL	Injection, EmulsionIntramuscular, Intravenous, Subcutaneous	Sagent Pharmaceuticals	25021-505	25021-0505-70
phytonadione	Phytonadione 1 mg/.5mL	Injection, EmulsionIntramuscular, Intravenous, Subcutaneous	Amneal Pharmaceuticals LLC	70121-1682	70121-1682-07
Phytonadione	Phytonadione 1 mg/.5mL	Injection, EmulsionIntramuscular, Intravenous, Subcutaneous	Alembic Pharmaceuticals Limited	46708-826	46708-0826-0546708-0826-10
Phytonadione	Phytonadione 1 mg/.5mL	Injection, EmulsionIntramuscular, Intravenous, Subcutaneous	Alembic Pharmaceuticals Inc.	62332-826	62332-0826-0562332-0826-10
Phytonadione	Phytonadione 5 mg/1	TabletOral	Coupler LLC	67046-1581	67046-1581-03

All 32 Phytonadione NDCs

Other NDCs under ANDA 210189

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

FDA NDC Directory listings under ANDA 210189
Product	Strength	Form · route	Labeler	Product NDC
Phytonadione	Phytonadione 5 mg/1	TabletOral	Northstar Rx LLC.	16714-973
Phytonadione	Phytonadione 5 mg/1	TabletOral	Safecor Health, LLC	48433-160
Phytonadione	Phytonadione 5 mg/1	TabletOral	Coupler LLC	67046-1581
Phytonadione	Phytonadione 5 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1318