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EVEROLIMUS

NDC 70377-010, everolimus, tablet, from Biocon Pharma Inc..

Product NDC
70377-010
Status
Listed
Labeler
Biocon Pharma Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214182
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70377-010 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • EVEROLIMUS2.5 mg/1

Pharmacologic classes

Cytochrome P450 2D6 Inhibitors [MoA]; Cytochrome P450 3A4 Inhibitors [MoA]; Decreased Immunologic Activity [PE]; Kinase Inhibitor [EPC]; Protein Kinase Inhibitors [MoA]; mTOR Inhibitor Immunosuppressant [EPC]; mTOR Inhibitors [MoA]

Package NDCNDC-11Package
70377-010-117037700101130 TABLET in 1 BOTTLE (70377-010-11)
70377-010-22703770010224 BLISTER PACK in 1 CARTON (70377-010-22) / 7 TABLET in 1 BLISTER PACK
70377-010-23703770010234 BLISTER PACK in 1 CARTON (70377-010-23) / 7 TABLET in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5fb55800-f322-6bb6-9dde-622925ef28bd

Use it

Look up 70377-010 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70377-010 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70377-010. 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.