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NEVIRAPINE

NDC 42571-131, NEVIRAPINE, tablet, from Micro Labs Limited.

Product NDC
42571-131
Status
Listed
Labeler
Micro Labs Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203080
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42571-131 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NEVIRAPINE200 mg/1

Pharmacologic classes

Cytochrome P450 2B6 Inducers [MoA]; Cytochrome P450 3A Inducers [MoA]; Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]; Non-Nucleoside Analog [EXT]; Non-Nucleoside Reverse Transcriptase Inhibitors [MoA]

Package NDCNDC-11Package
42571-131-29425710131296 BLISTER PACK in 1 CARTON (42571-131-29) / 10 TABLET in 1 BLISTER PACK
42571-131-604257101316060 TABLET in 1 BOTTLE (42571-131-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fbd628db-4076-4fe0-8323-9cc33ae92e42

Use it

Look up 42571-131 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42571-131 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42571-131. 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.