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Sodium Oxybate

NDC 65162-065, Sodium Oxybate, solution, from Amneal Pharmaceuticals LLC.

Product NDC
65162-065
Status
Listed
Labeler
Amneal Pharmaceuticals LLC
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203631
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65162-065 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM OXYBATE500 mg/mL

Pharmacologic classes

Central Nervous System Depressant [EPC]; Central Nervous System Depression [PE]; Decreased Central Nervous System Organized Electrical Activity [PE]

Package NDCNDC-11Package
65162-065-87651620065871 BOTTLE in 1 CARTON (65162-065-87) / 180 mL in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5a9e9045-f04d-46eb-8396-2495c6090a31

Use it

Look up 65162-065 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65162-065 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65162-065. 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.