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Emtricitabine and tenofovir disoproxil fumarate

NDC 70710-1366, Emtricitabine and tenofovir disoproxil fumarate, tablet, film coated, from Zydus Pharmaceuticals USA Inc..

Product NDC
70710-1366
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212689
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1366 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • EMTRICITABINE167 mg/1
  • TENOFOVIR DISOPROXIL FUMARATE250 mg/1

Pharmacologic classes

Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]; Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]; Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]; Nucleoside Reverse Transcriptase Inhibitors [MoA]; Nucleoside Reverse Transcriptase Inhibitors [MoA]; Nucleosides [CS]; Nucleosides [CS]

Package NDCNDC-11Package
70710-1366-37071013660330 TABLET, FILM COATED in 1 BOTTLE (70710-1366-3)
70710-1366-47071013660410 BLISTER PACK in 1 CARTON (70710-1366-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70710-1366-2)
70710-1366-97071013660990 TABLET, FILM COATED in 1 BOTTLE (70710-1366-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7def7a95-e69e-4985-974a-efacadcecc95

Use it

Look up 70710-1366 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1366 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70710-1366. 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.