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Lamivudine and Zidovudine

NDC 76282-115, Lamivudine and Zidovudine, tablet, film coated, from Exelan Pharmaceuticals Inc..

Product NDC
76282-115
Status
Listed
Labeler
Exelan Pharmaceuticals Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203259
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76282-115 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LAMIVUDINE150 mg/1
  • ZIDOVUDINE300 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 Analog [EXT]; Nucleoside Analog [EXT]; Nucleoside Reverse Transcriptase Inhibitors [MoA]; Nucleoside Reverse Transcriptase Inhibitors [MoA]

Package NDCNDC-11Package
76282-115-0576282011505500 TABLET, FILM COATED in 1 BOTTLE (76282-115-05)
76282-115-607628201156060 TABLET, FILM COATED in 1 BOTTLE (76282-115-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4cf565c3-bdec-4c18-93c1-cc7fa8331c90

Use it

Look up 76282-115 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76282-115 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76282-115. 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.