NDC codes

FDA NDC Directory
Product NDC (as listed)43386-771Labeler and product segments. Claims need a package NDC.
Product NDC at billing width43386-0771Add 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
43386-771-0143386077101100 CAPSULE in 1 BOTTLE (43386-771-01)Marketed from Jul 7, 2017 · Sample package

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)
Flucytosine
Generic name (nonproprietary)
flucytosine
Active ingredients
Flucytosine — 250 mg/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 204652
Marketing start
Listing expires
Other FDA classes
Nucleoside Analog (EXT)
Identifiers
Product ID 43386-771_f404c3d3-ea62-4918-aebd-58b00b661bb9SPL ID f404c3d3-ea62-4918-aebd-58b00b661bb9SPL set ID 5721b46a-4a9f-46c2-8804-a9bad4d5f80aRxCUI 197702, 197703UNII D83282DT06UPC 0343386770014, 0343386771035
Pharmacologic class
Nucleoside Analog Antifungal

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

N443386077101 followed by a unit qualifier and the quantity

Package 43386-0771-01. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Flucytosine Capsules USP is indicated only in the treatment of serious infections caused by susceptible strains of Candida and/or Cryptococcus . Candida: Septicemia, endocarditis and urinary system infections have been effectively treated with flucytosine. Limited trials in pulmonary infections justify the use of flucytosine. Cryptococcus: Meningitis and pulmonary infections have been treated effectively. Studies in septicemias and urinary tract infections are limited, but good responses have been reported. Flucytosine Capsules USP should be used in combination with amphotericin B for the treatment of systemic candidiasis and cryptococcosis because of the emergence of r…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 204652

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

FDA NDC Directory listings under ANDA 204652
ProductStrengthForm · routeLabelerProduct NDC
FlucytosineFlucytosine 500 mg/1CapsuleOralLupin Pharmaceuticals,Inc.43386-770
FlucytosineFlucytosine 250 mg/1CapsuleOralAvPAK50268-331
FlucytosineFlucytosine 500 mg/1CapsuleOralAvPAK50268-332
FlucytosineFlucytosine 250 mg/1CapsuleOralMajor Pharmaceuticals0904-6834
FlucytosineFlucytosine 500 mg/1CapsuleOralMajor Pharmaceuticals0904-6835
FlucytosineFlucytosine 250 mg/1CapsuleOralNovel Laboratories, Inc.40032-771
FlucytosineFlucytosine 500 mg/1CapsuleOralNovel Laboratories, Inc.40032-770

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