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Maraviroc

NDC 68475-008, Maraviroc, tablet, film coated, from Navinta LLC.

Product NDC
68475-008
Status
Listed
Labeler
Navinta LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217880
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68475-008 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MARAVIROC150 mg/1

Pharmacologic classes

CCR5 Co-receptor Antagonist [EPC]; Chemokine Co-receptor 5 Antagonists [MoA]

Package NDCNDC-11Package
68475-008-016847500080160 TABLET, FILM COATED in 1 BOTTLE (68475-008-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/211290a4-5e26-4784-aa99-8ccaf2eaaa15

Use it

Look up 68475-008 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68475-008 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68475-008. 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.