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NDC 52652-6001, baclofen, suspension, from Azurity Pharmaceuticals, Inc..

Product NDC
52652-6001
Status
Listed
Labeler
Azurity Pharmaceuticals, Inc.
Dosage form
SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA215602
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/52652-6001 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BACLOFEN5 mg/mL

Pharmacologic classes

GABA A Agonists [MoA]; GABA B Agonists [MoA]; gamma-Aminobutyric Acid-ergic Agonist [EPC]

Package NDCNDC-11Package
52652-6001-1526526001011 BOTTLE in 1 CARTON (52652-6001-1) / 120 mL in 1 BOTTLE
52652-6001-2526526001021 BOTTLE in 1 CARTON (52652-6001-2) / 300 mL in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9076d6ce-bbc2-4a9f-9cb9-2de1b675b9aa

  • NADAC price for package 52652600101

    GET /v1/drugs/nadac/52652600101

Use it

Look up 52652-6001 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/52652-6001 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 52652-6001. 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.