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Topiramate

NDC 62756-712, Topiramate, tablet, film coated, from Sun Pharmaceutical Industries, Inc..

Product NDC
62756-712
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090278
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62756-712 \
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Product

Active ingredients and packages

Active ingredients

  • TOPIRAMATE200 mg/1

Pharmacologic classes

Cytochrome P450 2C19 Inhibitors [MoA]; Cytochrome P450 3A4 Inducers [MoA]; Decreased Central Nervous System Disorganized Electrical Activity [PE]

Package NDCNDC-11Package
62756-712-0862756071208100 TABLET, FILM COATED in 1 BOTTLE (62756-712-08)
62756-712-1362756071213500 TABLET, FILM COATED in 1 BOTTLE (62756-712-13)
62756-712-18627560712181000 TABLET, FILM COATED in 1 BOTTLE (62756-712-18)
62756-712-836275607128330 TABLET, FILM COATED in 1 BOTTLE (62756-712-83)
62756-712-866275607128660 TABLET, FILM COATED in 1 BOTTLE (62756-712-86)
62756-712-8862756071288100 TABLET, FILM COATED in 1 BOTTLE (62756-712-88)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 62756-712 from code or an agent

curl
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  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.