Unfinished product

This listing is a drug for further processing, not a finished drug product dispensed or administered to patients. It is not normally billed.

NDC codes

FDA NDC Directory
Product NDC (as listed)0093-8117Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00093-8117Add 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
0093-8117-990009381179990909 TABLET, FILM COATED in 1 PAIL (0093-8117-99)Marketed from 23-JUN-23

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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

Generic name (nonproprietary)
famciclovir
Active ingredients
Famciclovir — 125 mg/1
Dosage form
Tablet, Film coated
Labeler
Teva Pharmaceuticals USA, Inc.NDC labeler code 0093
Product type
Drug for further processing
Marketing category
Drug for further processing
Marketing start
Listing expires
Identifiers
Product ID 0093-8117_c62597c7-f518-4229-9753-3509d9ccaa91SPL ID c62597c7-f518-4229-9753-3509d9ccaa91

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N400093811799 followed by a unit qualifier and the quantity

Package 00093-8117-99. 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 0093-8117

What is NDC 0093-8117?
0093-8117 is the product NDC for Famciclovir, Famciclovir 125 mg/1 tablet, film coated, listed with the FDA by Teva Pharmaceuticals USA, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Famciclovir.
What is the active ingredient?
Famciclovir.
Who is the labeler?
Teva Pharmaceuticals USA, Inc., NDC labeler code 0093. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Famciclovir?
21 other product NDCs are listed under this name. See all Famciclovir 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 Famciclovir NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
FamciclovirFamciclovir 125 mg/1Tablet, Film coatedOralAvKARE73190-09173190-0091-30
FamciclovirFamciclovir 250 mg/1Tablet, Film coatedOralAvKARE73190-09273190-0092-30
FamciclovirFamciclovir 500 mg/1Tablet, Film coatedOralAvKARE73190-09373190-0093-30
FamciclovirFamciclovir 125 mg/1Tablet, Film coatedOralAvKARE42291-41442291-0414-30
FamciclovirFamciclovir 250 mg/1Tablet, Film coatedOralAvKARE42291-41542291-0415-30
FamciclovirFamciclovir 500 mg/1Tablet, Film coatedOralAvKARE42291-41642291-0416-30
FamciclovirFamciclovir 125 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-70631722-0706-0131722-0706-0531722-0706-10+2 more
FamciclovirFamciclovir 250 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-70731722-0707-0131722-0707-0531722-0707-10+2 more
FamciclovirFamciclovir 500 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-70831722-0708-0131722-0708-0531722-0708-10+2 more
FamciclovirFamciclovir 500 mg/1Tablet, Film coatedOralProficient Rx LP63187-99863187-0998-2163187-0998-3063187-0998-60+1 more

All 22 Famciclovir NDCs

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