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gabapentin

NDC 70771-1862, gabapentin, tablet, from Zydus Lifesciences Limited.

Product NDC
70771-1862
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203934
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1862 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GABAPENTIN600 mg/1

Pharmacologic classes

Decreased Central Nervous System Disorganized Electrical Activity [PE]

Package NDCNDC-11Package
70771-1862-47077118620410 BLISTER PACK in 1 CARTON (70771-1862-4) / 10 TABLET in 1 BLISTER PACK (70771-1862-2)
70771-1862-570771186205500 TABLET in 1 BOTTLE (70771-1862-5)
70771-1862-97077118620990 TABLET in 1 BOTTLE (70771-1862-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8c0eeefc-ef5b-49f4-8411-ddbae312ed05

Use it

Look up 70771-1862 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1862 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1862. 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.