NDC codes

FDA NDC Directory
Product NDC (as listed)50090-0638Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-0638Add 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
50090-0638-0500900638005009006380035 TABLET in 1 BOTTLE (50090-0638-0)Marketed from Nov 28, 2014
50090-0638-2500900638025009006380270 TABLET in 1 BOTTLE (50090-0638-2)Marketed from Nov 28, 2014

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)
Acyclovir
Generic name (nonproprietary)
acyclovir
Active ingredients
Acyclovir — 800 mg/1
Dosage form
Tablet
Route
Oral
Labeler
A-S Medication SolutionsNDC labeler code 50090
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 075382
Marketing start
Listing expires
Other FDA classes
DNA Polymerase Inhibitors (Mechanism)Nucleoside Analog (EXT)
Identifiers
Product ID 50090-0638_4f4b014f-ecac-4563-b9a2-047423e25dceSPL ID 4f4b014f-ecac-4563-b9a2-047423e25dce
Pharmacologic class
Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor; Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor; Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor

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

N450090063800 followed by a unit qualifier and the quantity

Package 50090-0638-00. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 50090-0638

What is NDC 50090-0638?
50090-0638 is the product NDC for Acyclovir, Acyclovir 800 mg/1 tablet, listed with the FDA by A-S Medication Solutions. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Acyclovir.
What is the active ingredient?
Acyclovir.
Who is the labeler?
A-S Medication Solutions, NDC labeler code 50090. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Acyclovir?
193 other product NDCs are listed under this name. See all Acyclovir 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 Acyclovir NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
acyclovirAcyclovir 50 mg/gOintmentTopicalc68788-414268788-4142-01
AcyclovirAcyclovir 200 mg/1CapsuleOralCardinal Health 107, LLC55154-019955154-0199-00
acyclovirAcyclovir 800 mg/1TabletOralNorthwind Health Company, LLC82868-10782868-0107-3082868-0107-35
AcyclovirAcyclovir 50 mg/gOintmentTopicalAryeh Pharma Corp85957-03685957-0036-0185957-0036-0285957-0036-03
AcyclovirAcyclovir 200 mg/1CapsuleOralAvet Pharmaceuticals Inc.23155-96223155-0962-0123155-0962-05
AcyclovirAcyclovir 200 mg/1CapsuleOralFlorida Pharmaceutical Products, LLC71921-14671921-0146-01
AcyclovirAcyclovir 200 mg/1CapsuleOralMajor Pharmaceuticals0904-751900904-7519-61
AcyclovirAcyclovir 400 mg/1TabletOralAurobindo Pharma Limited59651-96559651-0965-0159651-0965-0559651-0965-10
AcyclovirAcyclovir 800 mg/1TabletOralAurobindo Pharma Limited59651-96659651-0966-0159651-0966-0559651-0966-10
AcyclovirAcyclovir 800 mg/1TabletOralREMEDYREPACK INC.70518-445070518-4450-0070518-4450-01

All 194 Acyclovir NDCs

Other NDCs under ANDA 075382

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

FDA NDC Directory listings under ANDA 075382
ProductStrengthForm · routeLabelerProduct NDC
AcyclovirAcyclovir 400 mg/1TabletOralAvPAK50268-061
AcyclovirAcyclovir 800 mg/1TabletOralAvPAK50268-062
AcyclovirAcyclovir 400 mg/1TabletOralGolden State Medical Supply, Inc.51407-145
AcyclovirAcyclovir 800 mg/1TabletOralGolden State Medical Supply, Inc.51407-146
AcyclovirAcyclovir 400 mg/1TabletOralCardinal Health 107, LLC55154-4332
AcyclovirAcyclovir 400 mg/1TabletOralCarlsbad Technology, Inc.61442-112
AcyclovirAcyclovir 800 mg/1TabletOralCarlsbad Technology, Inc.61442-113
AcyclovirAcyclovir 800 mg/1TabletOralBryant Ranch Prepack63629-1678
AcyclovirAcyclovir 800 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-2408
AcyclovirAcyclovir 400 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-2447
AcyclovirAcyclovir 800 mg/1TabletOralProficient Rx LP71205-053
AcyclovirAcyclovir 400 mg/1TabletOralProficient Rx LP71205-056
AcyclovirAcyclovir 400 mg/1TabletOralBryant Ranch Prepack71335-1053
AcyclovirAcyclovir 400 mg/1TabletOralBryant Ranch Prepack71335-2229
AcyclovirAcyclovir 800 mg/1TabletOralBryant Ranch Prepack71335-9721
AcyclovirAcyclovir 400 mg/1TabletOralBryant Ranch Prepack72162-1735

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