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NDC 53045-201, Sodium Fluoride, gel, from Dharma Research, inc..

Product NDC
53045-201
Status
Listed
Labeler
Dharma Research, inc.
Dosage form
GEL
Route
DENTAL, ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/53045-201 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM FLUORIDE10.241 g/490g
Package NDCNDC-11Package
53045-201-0853045020108245 g in 1 BOTTLE (53045-201-08)
53045-201-1753045020117490 g in 1 BOTTLE (53045-201-17)
53045-201-38530450201383724 g in 1 BOTTLE (53045-201-38)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8ff1b377-0535-4548-a109-f9f1a43b85b7

Use it

Look up 53045-201 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/53045-201 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 53045-201. 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.