NDC codes

FDA NDC Directory
Product NDC (as listed)0085-1430Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00085-1430Add 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
0085-1430-0300085143003000851430035 PACKET in 1 CARTON (0085-1430-03) / 1 CAPSULE in 1 PACKET (0085-1430-05)Marketed from Aug 11, 1999
0085-1430-04000851430040008514300414 PACKET in 1 CARTON (0085-1430-04) / 1 CAPSULE in 1 PACKET (0085-1430-05)Marketed from Aug 11, 1999

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

Brand name (proprietary)
Temodar
Generic name (nonproprietary)
temozolomide
Active ingredients
Temozolomide — 180 mg/1
Dosage form
Capsule
Route
Oral
Labeler
Merck Sharp & Dohme LLCNDC labeler code 0085
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 021029
Marketing start
Listing expires
Other FDA classes
Alkylating Activity (Mechanism)
Identifiers
Product ID 0085-1430_40ceddc0-83a2-4b3b-8953-fd0078a41133SPL ID 40ceddc0-83a2-4b3b-8953-fd0078a41133SPL set ID 046a9011-3911-4d3f-a15f-fbb56d5aad56RxCUI 261288, 261289, 261290, 261291, 313209, 313210, 313211, 317160, 700883, 700885, 705617, 705619, 835945, 835948UNII YF1K15M17Y
Pharmacologic class
Alkylating Drug

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

N400085143003 followed by a unit qualifier and the quantity

Package 00085-1430-03. 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)

TEMODAR is an alkylating drug indicated for the treatment of adults with: Newly diagnosed glioblastoma concomitantly with radiotherapy and then as maintenance treatment. ( 1.1 ) Anaplastic astrocytoma. ( 1.2 ) Adjuvant treatment of adults with newly diagnosed anaplastic astrocytoma. ( 1.2 ) Treatment of adults with refractory anaplastic astrocytoma. ( 1.2 ) 1.1 Newly Diagnosed Glioblastoma TEMODAR is indicated for the treatment of adults with newly diagnosed glioblastoma, concomitantly with radiotherapy and then as maintenance treatment. 1.2 Anaplastic Astrocytoma TEMODAR is indicated for the: adjuvant treatment of adults with newly diagnosed anaplastic astrocytoma; treatment of adults with …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0085-1430

What is NDC 0085-1430?
0085-1430 is the product NDC for Temodar (temozolomide), Temozolomide 180 mg/1 capsule, listed with the FDA by Merck Sharp & Dohme LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Temodar (Temozolomide).
What is the active ingredient?
Temozolomide.
Who is the labeler?
Merck Sharp & Dohme LLC, NDC labeler code 0085. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Temodar?
6 other product NDCs are listed under this name. See all Temodar 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 Temodar NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
TemodartemozolomideTemozolomide 2.5 mg/mLInjection, Powder, Lyophilized, For solutionIntravenousMerck Sharp & Dohme LLC0085-138100085-1381-01
TemodartemozolomideTemozolomide 100 mg/1CapsuleOralMerck Sharp & Dohme LLC0085-136600085-1366-0300085-1366-04
TemodartemozolomideTemozolomide 250 mg/1CapsuleOralMerck Sharp & Dohme LLC0085-141700085-1417-02
TemodartemozolomideTemozolomide 140 mg/1CapsuleOralMerck Sharp & Dohme LLC0085-142500085-1425-0300085-1425-04
TemodartemozolomideTemozolomide 20 mg/1CapsuleOralMerck Sharp & Dohme LLC0085-151900085-1519-0300085-1519-04
TemodartemozolomideTemozolomide 5 mg/1CapsuleOralMerck Sharp & Dohme LLC0085-300400085-3004-0300085-3004-04

Other NDCs under NDA 021029

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

FDA NDC Directory listings under NDA 021029
ProductStrengthForm · routeLabelerProduct NDC
TemodartemozolomideTemozolomide 100 mg/1CapsuleOralMerck Sharp & Dohme LLC0085-1366
TemodartemozolomideTemozolomide 250 mg/1CapsuleOralMerck Sharp & Dohme LLC0085-1417
TemodartemozolomideTemozolomide 140 mg/1CapsuleOralMerck Sharp & Dohme LLC0085-1425
TemodartemozolomideTemozolomide 20 mg/1CapsuleOralMerck Sharp & Dohme LLC0085-1519
TemodartemozolomideTemozolomide 5 mg/1CapsuleOralMerck Sharp & Dohme LLC0085-3004

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