NDC codes

FDA NDC Directory
Product NDC (as listed)16729-267Labeler and product segments. Claims need a package NDC.
Product NDC at billing width16729-0267Add 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
16729-267-6316729026763167290267631 VIAL, MULTI-DOSE in 1 CARTON (16729-267-63) / 1 mL in 1 VIAL, MULTI-DOSEMarketed from Oct 22, 2013
16729-267-6416729026764167290267641 VIAL, MULTI-DOSE in 1 CARTON (16729-267-64) / 4 mL in 1 VIAL, MULTI-DOSEMarketed from Aug 2, 2013
16729-267-6516729026765167290267651 VIAL, MULTI-DOSE in 1 CARTON (16729-267-65) / 8 mL in 1 VIAL, MULTI-DOSEMarketed from May 30, 2013

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)
Docetaxel
Generic name (nonproprietary)
docetaxel
Active ingredients
Docetaxel anhydrous — 20 mg/mL
Dosage form
Injection, Solution, Concentrate
Route
Intravenous
Labeler
Accord Healthcare Inc.NDC labeler code 16729
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 201195
Marketing start
Listing expires
Other FDA classes
Microtubule Inhibition (Physiologic effect)
Identifiers
Product ID 16729-267_1fbda3cb-1ba1-490d-e063-6294a90a6777SPL ID 1fbda3cb-1ba1-490d-e063-6294a90a6777SPL set ID f59f7811-70b7-4c44-99f7-4f4fdce3ed22RxCUI 1001405UNII 699121PHCAUPC 0316729267656
Pharmacologic class
Microtubule 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 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.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N416729026763 followed by a unit qualifier and the quantity

Package 16729-0267-63. 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)

Docetaxel Injection is a microtubule inhibitor indicated for: Breast Cancer (BC) : single agent for locally advanced or metastatic BC after chemotherapy failure; and with doxorubicin and cyclophosphamide as adjuvant treatment of operable node-positive BC ( 1.1 ) Non-small Cell Lung Cancer (NSCLC) : single agent for locally advanced or metastatic NSCLC after platinum therapy failure; and with cisplatin for unresectable, locally advanced or metastatic untreated NSCLC ( 1.2 ) Castration-Resistant Prostate Cancer (CRPC) : with prednisone in metastatic castration-resistant prostate cancer ( 1.3 ) Gastric Adenocarcinoma (GC) : with cisplatin and fluorouracil for untreated, advanced GC, including t…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 16729-267

What is NDC 16729-267?
16729-267 is the product NDC for Docetaxel, Docetaxel anhydrous 20 mg/mL injection, solution, concentrate, listed with the FDA by Accord Healthcare Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Docetaxel.
What is the active ingredient?
Docetaxel anhydrous.
Who is the labeler?
Accord Healthcare Inc., NDC labeler code 16729. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Docetaxel?
61 other product NDCs are listed under this name. See all Docetaxel 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 Docetaxel NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
DocetaxelDocetaxel anhydrous 10 mg/mLInjectionIntravenousBaxter Healthcare Corporation43066-04443066-0044-02
DocetaxelDocetaxel anhydrous 10 mg/mLInjectionIntravenousBaxter Healthcare Corporation43066-04643066-0046-08
DocetaxelDocetaxel anhydrous 10 mg/mLInjectionIntravenousBaxter Healthcare Corporation43066-04843066-0048-16
DocetaxelDocetaxel 20 mg/mLInjection, Solution, ConcentrateIntravenousMeitheal Pharmaceuticals Inc.71288-13371288-0133-01
DocetaxelDocetaxel 20 mg/mLInjection, Solution, ConcentrateIntravenousMeitheal Pharmaceuticals Inc.71288-15271288-0152-04
DocetaxelDocetaxel 20 mg/mLInjectionIntravenousHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-90323155-0903-31
DocetaxelDocetaxel 80 mg/4mLInjectionIntravenousHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-90423155-0904-31
DocetaxelDocetaxel 160 mg/8mLInjectionIntravenousHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-90523155-0905-31
Docetaxeldocetaxel anhydrousDocetaxel anhydrous 10 mg/mLInjectionIntravenousSagent Pharmaceuticals25021-25425021-0254-0825021-0254-16
DocetaxelDocetaxel anhydrous 10 mg/mLInjectionIntravenousAlembic Pharmaceuticals Limited46708-67846708-0678-0246708-0678-0846708-0678-16

All 62 Docetaxel NDCs

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