NDC codes

FDA NDC Directory
Product NDC (as listed)50090-5709Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-5709Add 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
50090-5709-05009057090030 CAPSULE in 1 BOTTLE (50090-5709-0)Marketed from Sep 24, 2021
50090-5709-35009057090360 CAPSULE in 1 BOTTLE (50090-5709-3)Marketed from Sep 24, 2021

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)
rifampin
Generic name (nonproprietary)
rifampin
Active ingredients
Rifampin — 300 mg/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 090034
Marketing start
Listing expires
Other FDA classes
Rifamycins (Chemical structure)
Identifiers
Product ID 50090-5709_37783510-9524-4bee-89d1-c96e36d6791aSPL ID 37783510-9524-4bee-89d1-c96e36d6791aSPL set ID d53b6998-6e3b-4c6f-8465-2af6897d1efeRxCUI 198202UNII VJT6J7R4TR
Pharmacologic class
Rifamycin 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

N450090570900 followed by a unit qualifier and the quantity

Package 50090-5709-00. 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 In the treatment of both tuberculosis and the meningococcal carrier state, the small number of resistant cells present within large populations of susceptible cells can rapidly become the predominant type. Bacteriologic cultures should be obtained before the start of therapy to confirm the susceptibility of the organism to rifampin and they should be repeated throughout therapy to monitor the response to treatment. Since resistance can emerge rapidly, susceptibility tests should be performed in the event of persistent positive cultures during the course of treatment. If test results show resistance to rifampin and the patient is not responding to therapy, the drug regim…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 090034

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

FDA NDC Directory listings under ANDA 090034
ProductStrengthForm · routeLabelerProduct NDC
rifampinRifampin 300 mg/1CapsuleOralBryant Ranch Prepack71335-2613
rifampinRifampin 150 mg/1CapsuleOralLupin Pharmaceuticals, Inc.68180-658
RifampinRifampin 150 mg/1CapsuleOralAmerican Health Packaging60687-575
rifampinRifampin 300 mg/1CapsuleOralLupin Pharmaceuticals, Inc.68180-659
RifampinRifampin 300 mg/1CapsuleOralAmerican Health Packaging60687-586
rifampinRifampin 300 mg/1CapsuleOralMajor Pharmaceuticals0904-7315

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