NDC codes

FDA NDC Directory
Product NDC (as listed)70518-0265Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-0265Add 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
70518-0265-3705180265037051802650310 CAPSULE in 1 BOTTLE, PLASTIC (70518-0265-3)Marketed from Sep 12, 2019

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

Generic name (nonproprietary)
nitrofurantoin monohydrate/macrocrystalline
Active ingredients
Nitrofurantoin — 25 mg/1Nitrofurantoin monohydrate — 75 mg/1
Dosage form
Capsule
Route
Oral
Labeler
REMEDYREPACK INC.NDC labeler code 70518
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 020064
Marketing start
Listing expires
Other FDA classes
Nitrofurans (Chemical structure)Nitrofurans (Chemical structure)
Identifiers
Product ID 70518-0265_5502c311-ea4a-559e-e063-6294a90af916SPL ID 5502c311-ea4a-559e-e063-6294a90af916SPL set ID a4afd48b-003f-4ffa-9ca0-9432b8b0e22bRxCUI 1648755UNII 927AH8112L, 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

N470518026503 followed by a unit qualifier and the quantity

Package 70518-0265-03. 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)

INDICATIONS AND USAGE Nitrofurantoin capsules (monohydrate/macrocrystals) are indicated only for the treatment of acute uncomplicated urinary tract infections (acute cystitis) caused by susceptible strains of Escherichia coli or Staphylococcus saprophyticus . Nitrofurantoin is not indicated for the treatment of pyelonephritis or perinephric abscesses. To reduce the development of drug-resistant bacteria and maintain the effectiveness of nitrofurantoin capsules (monohydrate/macrocrystals) and other antibacterial drugs, nitrofurantoin capsules (monohydrate/macrocrystals) should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteri…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70518-0265

What is NDC 70518-0265?
70518-0265 is the product NDC for Nitrofurantoin Monohydrate/ Macrocrystalline, Nitrofurantoin 25 mg/1; Nitrofurantoin monohydrate 75 mg/1 capsule, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Nitrofurantoin Monohydrate/ Macrocrystalline (Nitrofurantoin Monohydrate/Macrocrystalline).
What is the active ingredient?
Nitrofurantoin, Nitrofurantoin monohydrate.
Who is the labeler?
REMEDYREPACK INC., NDC labeler code 70518. 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 Monohydrate/ Macrocrystalline?
3 other product NDCs are listed under this name. See all Nitrofurantoin Monohydrate/ Macrocrystalline 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 Monohydrate/ Macrocrystalline NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Nitrofurantoin Monohydrate Macrocrystallinenitrofurantoin monohydrateNitrofurantoin 25 mg/1; Nitrofurantoin monohydrate 75 mg/1CapsuleOralDirect_Rx61919-02161919-0021-0261919-0021-1061919-0021-14
Nitrofurantoin Monohydrate/ Macrocrystallinenitrofurantoin monohydrate/macrocrystallineNitrofurantoin 25 mg/1; Nitrofurantoin monohydrate 75 mg/1CapsuleOralAlvogen Inc.47781-30347781-0303-01
Nitrofurantoin Monohydrate/ Macrocrystallinenitrofurantoin monohydrate/macrocrystallineNitrofurantoin 25 mg/1; Nitrofurantoin monohydrate 75 mg/1CapsuleOralProficient Rx LP63187-26363187-0263-1063187-0263-1463187-0263-28+2 more

Other NDCs under NDA 020064

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

FDA NDC Directory listings under NDA 020064
ProductStrengthForm · routeLabelerProduct NDC
Macrobidnitrofurantoin monohydrate/macrocrystallineNitrofurantoin 25 mg/1; Nitrofurantoin monohydrate 75 mg/1CapsuleOralAlmatica Pharma LLC52427-285
Macrobidnitrofurantoin monohydrate/macrocrystallineNitrofurantoin 25 mg/1; Nitrofurantoin monohydrate 75 mg/1CapsuleOralREMEDYREPACK INC.70518-2531
Nitrofurantoin Mononitrofurantoin monohydrateNitrofurantoin monohydrate 75 mg/1; Nitrofurantoin 25 mg/1CapsuleOralPharmPak, Inc.54348-849
Nitrofurantoin Monohydrate Macrocrystallinenitrofurantoin monohydrateNitrofurantoin 25 mg/1; Nitrofurantoin monohydrate 75 mg/1CapsuleOralDirect_Rx61919-021
Nitrofurantoin Monohydrate/ Macrocrystallinenitrofurantoin monohydrate/macrocrystallineNitrofurantoin 25 mg/1; Nitrofurantoin monohydrate 75 mg/1CapsuleOralAlvogen Inc.47781-303
Nitrofurantoin Monohydrate/ Macrocrystallinenitrofurantoin monohydrate/macrocrystallineNitrofurantoin 25 mg/1; Nitrofurantoin monohydrate 75 mg/1CapsuleOralProficient Rx LP63187-263

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