NDC codes

FDA NDC Directory
Product NDC (as listed)17772-102Labeler and product segments. Claims need a package NDC.
Product NDC at billing width17772-0102Add 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
17772-102-0117772010201100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (17772-102-01)Marketed from Aug 16, 2013
17772-102-07177720102077 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (17772-102-07)Marketed from Jun 23, 2020 · Sample package
17772-102-10177720102105 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (17772-102-10)Marketed from Aug 16, 2013 · Sample package
17772-102-12177720102127 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (17772-102-12)Marketed from Aug 16, 2013 · Sample package
17772-102-301777201023030 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (17772-102-30)Marketed from Aug 16, 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)
Trokendi XR
Generic name (nonproprietary)
topiramate
Active ingredients
Topiramate — 50 mg/1
Dosage form
Capsule, Extended release
Route
Oral
Labeler
Supernus Pharmaceuticals, Inc.NDC labeler code 17772
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 201635
Marketing start
Listing expires
Other FDA classes
Cytochrome P450 2C19 Inhibitors (Mechanism)Cytochrome P450 3A4 Inducers (Mechanism)Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers
Product ID 17772-102_5b8a1778-ed48-a5a4-e063-6394a90a581cSPL ID 5b8a1778-ed48-a5a4-e063-6394a90a581c

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

N417772010201 followed by a unit qualifier and the quantity

Package 17772-0102-01. 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 17772-102

What is NDC 17772-102?
17772-102 is the product NDC for Trokendi XR (topiramate), Topiramate 50 mg/1 capsule, extended release, listed with the FDA by Supernus Pharmaceuticals, Inc.. It has 5 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Trokendi XR (Topiramate).
What is the active ingredient?
Topiramate.
Who is the labeler?
Supernus Pharmaceuticals, Inc., NDC labeler code 17772. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Trokendi XR?
3 other product NDCs are listed under this name. See all Trokendi XR 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 Trokendi XR NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Trokendi XRtopiramateTopiramate 25 mg/1Capsule, Extended releaseOralSupernus Pharmaceuticals, Inc.17772-10117772-0101-0117772-0101-0717772-0101-10+2 more
Trokendi XRtopiramateTopiramate 100 mg/1Capsule, Extended releaseOralSupernus Pharmaceuticals, Inc.17772-10317772-0103-0117772-0103-0717772-0103-10+2 more
Trokendi XRtopiramateTopiramate 200 mg/1Capsule, Extended releaseOralSupernus Pharmaceuticals, Inc.17772-10417772-0104-0117772-0104-0717772-0104-10+2 more

Other NDCs under NDA 201635

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

FDA NDC Directory listings under NDA 201635
ProductStrengthForm · routeLabelerProduct NDC
Trokendi XRtopiramateTopiramate 25 mg/1Capsule, Extended releaseOralSupernus Pharmaceuticals, Inc.17772-101
Trokendi XRtopiramateTopiramate 100 mg/1Capsule, Extended releaseOralSupernus Pharmaceuticals, Inc.17772-103
Trokendi XRtopiramateTopiramate 200 mg/1Capsule, Extended releaseOralSupernus Pharmaceuticals, Inc.17772-104

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