gabapentin

NDC 68382-608, gabapentin, tablet, from Zydus Pharmaceuticals USA Inc..

Product NDC: 68382-608
Status: Listed
Labeler: Zydus Pharmaceuticals USA Inc.
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/68382-608 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

GABAPENTIN300 mg/1

Pharmacologic classes

Decreased Central Nervous System Disorganized Electrical Activity [PE]

Package NDC	NDC-11	Package
68382-608-05	68382060805	500 TABLET in 1 BOTTLE (68382-608-05)
68382-608-16	68382060816	90 TABLET in 1 BOTTLE (68382-608-16)
68382-608-77	68382060877	10 BLISTER PACK in 1 CARTON (68382-608-77) / 10 TABLET in 1 BLISTER PACK (68382-608-30)

Linked data

RxNorm, label and prices

RxNorm concepts

1806380Once-Daily gabapentin 300 MG Oral Tablet (SCD)

Related lookups

FDA label sections
GET /v1/drugs/labels/3cfd04ab-e421-441f-a10e-e4dd1412974d
NADAC price for package 68382060816
GET /v1/drugs/nadac/68382060816

Use it

Look up 68382-608 from code or an agent

curl

curl https://api.healthcare.dev/v1/drugs/ndc/68382-608 \
  -H "Authorization: Bearer $HDEV_API_KEY"

MCP prompt

Using the healthcare.dev MCP server, look up NDC 68382-608. 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.