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Emtricitabine and tenofovir disoproxil fumarate

NDC 70771-1621, Emtricitabine and tenofovir disoproxil fumarate, tablet, film coated, from Zydus Lifesciences Limited.

Product NDC
70771-1621
Status
Listed
Labeler
Zydus Lifesciences Limited
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/70771-1621 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • EMTRICITABINE133 mg/1
  • TENOFOVIR DISOPROXIL FUMARATE200 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
70771-1621-37077116210330 TABLET, FILM COATED in 1 BOTTLE (70771-1621-3)
70771-1621-47077116210410 BLISTER PACK in 1 CARTON (70771-1621-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1621-2)
70771-1621-97077116210990 TABLET, FILM COATED in 1 BOTTLE (70771-1621-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a0ee89b6-72c3-4b99-8d1c-d7473f1d5ef3

Use it

Look up 70771-1621 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1621 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1621. 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.