NDC codes

FDA NDC Directory
Product NDC (as listed)64980-593Labeler and product segments. Claims need a package NDC.
Product NDC at billing width64980-0593Add 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
64980-593-2464980059324649800593241 BOTTLE in 1 CARTON (64980-593-24) / 230 mL in 1 BOTTLEMarketed from May 11, 2023

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)
Nitrofurantoin
Generic name (nonproprietary)
nitrofurantoin
Active ingredients
Nitrofurantoin monohydrate — 25 mg/5mL
Dosage form
Suspension
Route
Oral
Labeler
Rising Pharma Holdings, Inc.NDC labeler code 64980
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 212607
Marketing start
Listing expires
Other FDA classes
Nitrofurans (Chemical structure)
Identifiers
Product ID 64980-593_dfecf83b-2b30-4505-9044-bec3dce43a39SPL ID dfecf83b-2b30-4505-9044-bec3dce43a39SPL set ID 11e700aa-66f9-4939-8a6b-a23240ae1a0bRxCUI 311989UNII E1QI2CQQ1I
Pharmacologic class
Nitrofuran Antibacterial

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

N464980059324 followed by a unit qualifier and the quantity

Package 64980-0593-24. 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)

Nitrofurantoin oral suspension is indicated in adults and pediatric patients 1 month of age and older for the treatment of urinary tract infections due to susceptible strains of Escherichia coli, Enterococcus species , Staphylococcus aureus, Klebsiella species and Enterobacter species. Limitations of Use Nitrofurantoin oral suspension is not indicated for the treatment of pyelonephritis or perinephric abscesses [see Warnings and Precautions (5.7) ]. Usage To reduce the development of drug-resistant bacteria and maintain the effectiveness of nitrofurantoin oral suspension and other antibacterial drugs, nitrofurantoin oral suspension should be used only to treat or prevent infections that are …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 64980-593

What is NDC 64980-593?
64980-593 is the product NDC for Nitrofurantoin, Nitrofurantoin monohydrate 25 mg/5mL suspension, listed with the FDA by Rising Pharma Holdings, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Nitrofurantoin.
What is the active ingredient?
Nitrofurantoin monohydrate.
Who is the labeler?
Rising Pharma Holdings, Inc., NDC labeler code 64980. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Nitrofurantoin?
43 other product NDCs are listed under this name. See all Nitrofurantoin 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 Nitrofurantoin NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
NitrofurantoinNitrofurantoin 25 mg/5mLSuspensionOralCamber Pharmaceuticals, Inc.31722-49131722-0491-23
NitrofurantoinNitrofurantoin 25 mg/5mLFor suspensionOralSomerset Therapeutics, LLC70069-82970069-0829-01
NitrofurantoinNitrofurantoin 100 mg/1CapsuleOralREMEDYREPACK INC.70518-424470518-4244-00
NitrofurantoinNitrofurantoin 25 mg/5mLSuspensionOralBiocon Pharma Inc70377-11870377-0118-31
NitrofurantoinNitrofurantoin 100 mg/1CapsuleOralMicro Labs Limited42571-39342571-0393-0142571-0393-0542571-0393-90
NitrofurantoinNitrofurantoin 50 mg/5mLSuspensionOralRising Pharma Holdings, Inc.16571-88816571-0888-06
nitrofurantoinnitrofurantoin macrocrystalsNitrofurantoin 100 mg/1CapsuleOralA-S Medication Solutions50090-721750090-7217-0050090-7217-0250090-7217-03
NitrofurantoinNitrofurantoin 25 mg/1; Nitrofurantoin monohydrate 75 mg/1CapsuleOralSt. Mary's Medical Park Pharmacy60760-85360760-0853-14
Nitrofurantoinnitrofurantoin (monohydrate/macrocrystals)Nitrofurantoin monohydrate 75 mg/1; Nitrofurantoin 25 mg/1CapsuleOralNuCare Pharmaceuticals,Inc.68071-356968071-3569-0168071-3569-0268071-3569-04
NitrofurantoinNitrofurantoin monohydrate 25 mg/5mLSuspensionOralAurobindo Pharma Limited59651-20659651-0206-23

All 44 Nitrofurantoin NDCs

Other NDCs under ANDA 212607

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

FDA NDC Directory listings under ANDA 212607
ProductStrengthForm · routeLabelerProduct NDC
NitrofurantoinNitrofurantoin monohydrate 25 mg/5mLSuspensionOralAurobindo Pharma Limited59651-206

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