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NDC 49702-204, lamivudine, tablet, film coated, from ViiV Healthcare Company.

Product NDC
49702-204
Status
Listed
Labeler
ViiV Healthcare Company
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA020564
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/49702-204 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LAMIVUDINE300 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
49702-204-134970202041330 TABLET, FILM COATED in 1 BOTTLE (49702-204-13)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/89226149-47fa-4f7d-bb1f-1aa7034486b8

Use it

Look up 49702-204 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/49702-204 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 49702-204. 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.