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gabapentin

NDC 62756-204, gabapentin, tablet, film coated, from Sun Pharmaceutical Industries, Inc..

Product NDC
62756-204
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077525
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62756-204 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GABAPENTIN800 mg/1

Pharmacologic classes

Decreased Central Nervous System Disorganized Electrical Activity [PE]

Package NDCNDC-11Package
62756-204-0162756020401100 TABLET, FILM COATED in 1 BOTTLE (62756-204-01)
62756-204-0362756020403500 TABLET, FILM COATED in 1 BOTTLE (62756-204-03)

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 62756-204 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62756-204 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62756-204. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.