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Lamivudine and Zidovudine

NDC 31722-739, Lamivudine and Zidovudine, tablet, film coated, from Camber Pharmaceuticals, Inc..

Product NDC
31722-739
Status
Listed
Labeler
Camber 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/31722-739 \
  -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 Reverse Transcriptase Inhibitors [MoA]; Nucleoside Reverse Transcriptase Inhibitors [MoA]

Package NDCNDC-11Package
31722-739-0531722073905500 TABLET, FILM COATED in 1 BOTTLE (31722-739-05)
31722-739-3131722073931100 TABLET, FILM COATED in 1 BLISTER PACK (31722-739-31)
31722-739-603172207396060 TABLET, FILM COATED in 1 BOTTLE (31722-739-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e816e8f5-1e50-4f49-8bea-92da0121d26e

Use it

Look up 31722-739 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/31722-739 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 31722-739. 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.