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Rilpivirine

NDC 42385-999, Rilpivirine, tablet, film coated, from Laurus Labs Limited.

Product NDC
42385-999
Status
Listed
Labeler
Laurus Labs Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA219788
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42385-999 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • RILPIVIRINE HYDROCHLORIDE25 mg/1

Pharmacologic classes

Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]; Non-Nucleoside Analog [EXT]; Non-Nucleoside Reverse Transcriptase Inhibitors [MoA]

Package NDCNDC-11Package
42385-999-304238509993030 TABLET, FILM COATED in 1 BOTTLE (42385-999-30)
42385-999-314238509993130 TABLET, FILM COATED in 1 BOTTLE (42385-999-31)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dadbf50d-6b7d-4fb5-bd9f-7769b048e764

Use it

Look up 42385-999 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42385-999 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42385-999. 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.