NDC codes

FDA NDC Directory
Product NDC (as listed)60687-381Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60687-0381Add 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
60687-381-946068703819420 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-381-94) / 1 TABLET in 1 BLISTER PACK (60687-381-11)Marketed from Jun 21, 2018

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)
Phytonadione
Generic name (nonproprietary)
phytonadione
Active ingredients
Phytonadione — 5 mg/1
Dosage form
Tablet
Route
Oral
Labeler
American Health PackagingNDC labeler code 60687
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209373
Marketing start
Listing expires
Other FDA classes
Increased Prothrombin Activity (Physiologic effect)Reversed Anticoagulation Activity (Physiologic effect)Vitamin K (Chemical structure)
Identifiers
Product ID 60687-381_22df1183-63b6-9572-e063-6394a90ae974SPL ID 22df1183-63b6-9572-e063-6394a90ae974SPL set ID 88d13044-6ce8-4374-86ff-e8d9eea27829RxCUI 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

N460687038194 followed by a unit qualifier and the quantity

Package 60687-0381-94. 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)

Phytonadione tablets are 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 absorpsion 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 defi…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 60687-381

What is NDC 60687-381?
60687-381 is the product NDC for Phytonadione, Phytonadione 5 mg/1 tablet, listed with the FDA by American Health Packaging. It has 1 package NDC, 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?
American Health Packaging, NDC labeler code 60687. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
PhytonadionePhytonadione 5 mg/1TabletOralSafecor Health, LLC48433-16048433-0160-03
PhytonadionePhytonadione 1 mg/.5mLInjection, EmulsionIntramuscular, Intravenous, SubcutaneousSun Pharmaceutical Industries, Inc.70095-15470095-0154-02
PhytonadionePhytonadione 10 mg/mLInjection, EmulsionIntramuscular, Intravenous, SubcutaneousAmneal Pharmaceuticals Private Limited80830-168380830-1683-03
PhytonadionePhytonadione 1 mg/.5mLInjection, EmulsionIntramuscular, Intravenous, SubcutaneousOrbicular Pharmaceutical Technologies Private Limited81607-02081607-0020-02
PhytonadionePhytonadione 1 mg/.5mLInjection, EmulsionIntramuscular, Intravenous, SubcutaneousBaxter Healthcare Corporation43066-13243066-0132-10
PhytonadionePhytonadione 1 mg/.5mLInjection, EmulsionIntramuscular, Intravenous, SubcutaneousSagent Pharmaceuticals25021-50525021-0505-70
phytonadionePhytonadione 1 mg/.5mLInjection, EmulsionIntramuscular, Intravenous, SubcutaneousAmneal Pharmaceuticals LLC70121-168270121-1682-07
PhytonadionePhytonadione 1 mg/.5mLInjection, EmulsionIntramuscular, Intravenous, SubcutaneousAlembic Pharmaceuticals Limited46708-82646708-0826-0546708-0826-10
PhytonadionePhytonadione 1 mg/.5mLInjection, EmulsionIntramuscular, Intravenous, SubcutaneousAlembic Pharmaceuticals Inc.62332-82662332-0826-0562332-0826-10
PhytonadionePhytonadione 5 mg/1TabletOralCoupler LLC67046-158167046-1581-03

All 32 Phytonadione NDCs

Other NDCs under ANDA 209373

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

FDA NDC Directory listings under ANDA 209373
ProductStrengthForm · routeLabelerProduct NDC
PhytonadionePhytonadione 5 mg/1TabletOralAmneal Pharmaceuticals NY LLC69238-1051
PhytonadionePhytonadione 5 mg/1TabletOralMajor Pharmaceuticals0904-6882

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