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Amoxicillin and Clavulanate Potassium

NDC 70518-3604, Amoxicillin and Clavulanate Potassium, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-3604
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA065096
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3604 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AMOXICILLIN875 mg/1
  • CLAVULANATE POTASSIUM125 mg/1

Pharmacologic classes

Penicillin-class Antibacterial [EPC]; Penicillins [CS]; beta Lactamase Inhibitor [EPC]; beta Lactamase Inhibitors [MoA]

Package NDCNDC-11Package
70518-3604-37051836040330 TABLET, FILM COATED in 1 BLISTER PACK (70518-3604-3)
70518-3604-47051836040420 TABLET, FILM COATED in 1 BLISTER PACK (70518-3604-4)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/aa77bab1-1c08-43bf-a943-0399646b3e1c

Use it

Look up 70518-3604 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3604 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3604. 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.