NDC codes

FDA NDC Directory
Product NDC (as listed)71335-9727Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-9727Add 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
71335-9727-07133597270028 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9727-0)Marketed from Apr 5, 2024
71335-9727-17133597270130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9727-1)Marketed from May 30, 2023
71335-9727-27133597270260 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9727-2)Marketed from Apr 5, 2024
71335-9727-37133597270390 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9727-3)Marketed from Jun 30, 2023
71335-9727-47133597270456 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9727-4)Marketed from Feb 20, 2024
71335-9727-57133597270584 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9727-5)Marketed from Apr 5, 2024
71335-9727-671335972706120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9727-6)Marketed from Aug 2, 2023
71335-9727-7713359727077 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9727-7)Marketed from Apr 5, 2024
71335-9727-87133597270814 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9727-8)Marketed from Apr 5, 2024
71335-9727-97133597270945 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9727-9)Marketed from Apr 5, 2024

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)
topiramate
Generic name (nonproprietary)
topiramate
Active ingredients
Topiramate — 25 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 090162
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 71335-9727_e00d0107-e233-4b4c-a837-9a2d0123c8b4SPL ID e00d0107-e233-4b4c-a837-9a2d0123c8b4SPL set ID 654f7c48-8c5d-4b97-88d6-397696f82b6aRxCUI 199888UNII 0H73WJJ391

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

N471335972700 followed by a unit qualifier and the quantity

Package 71335-9727-00. 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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Topiramate tablets are indicated for: Epilepsy: initial monotherapy for the treatment of partial-onset or primary generalized tonic-clonic seizures in patients 2 years of age and older (1.1); adjunctive therapy for the treatment of partial-onset seizures, primary generalized tonic-clonic seizures, or seizures associated with Lennox-Gastaut syndrome in patients 2 years of age and older ( 1.2 ) Preventive treatment of migraine in patients 12 years of age and older ( 1.3 ) 1.1 Monotherapy Epilepsy Topiramate tablets are indicated as initial monotherapy for the treatment of partial-onset or primary generalized tonic-clonic seizures in patients 2 years of age and older. 1.2 Adjunctive Therapy Epi…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 090162

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

FDA NDC Directory listings under ANDA 090162
ProductStrengthForm · routeLabelerProduct NDC
topiramateTopiramate 50 mg/1Tablet, Film coatedOralCoupler LLC67046-1202
topiramateTopiramate 100 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-2318
TopiramateTopiramate 50 mg/1Tablet, Film coatedOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0214
topiramateTopiramate 25 mg/1Tablet, Film coatedOralUnichem Pharmaceuticals (USA), Inc.29300-115
topiramateTopiramate 50 mg/1Tablet, Film coatedOralUnichem Pharmaceuticals (USA), Inc.29300-116
topiramateTopiramate 100 mg/1Tablet, Film coatedOralUnichem Pharmaceuticals (USA), Inc.29300-117
topiramateTopiramate 200 mg/1Tablet, Film coatedOralUnichem Pharmaceuticals (USA), Inc.29300-118
topiramateTopiramate 100 mg/1Tablet, Film coatedOralAdvanced Rx of Tennessee, LLC80425-0488
topiramateTopiramate 50 mg/1Tablet, Film coatedOralAdvanced Rx of Tennessee, LLC80425-0495
topiramateTopiramate 25 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7067
topiramateTopiramate 100 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-2482
topiramateTopiramate 25 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-2480
topiramateTopiramate 50 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-2481
topiramateTopiramate 200 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-2483
topiramateTopiramate 25 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-8817
topiramateTopiramate 25 mg/1Tablet, Film coatedOralSt. Mary's Medical Park Pharmacy60760-752
topiramateTopiramate 50 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-8828
topiramateTopiramate 25 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-3660
topiramateTopiramate 25 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-4515
topiramateTopiramate 100 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-8835

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