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Ammonium Lactate

NDC 51672-1300, Ammonium Lactate, lotion, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-1300
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
LOTION
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076216
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1300 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AMMONIUM LACTATE120 mg/g

Pharmacologic classes

Acidifying Activity [MoA]

Package NDCNDC-11Package
51672-1300-551672130005225 g in 1 BOTTLE, PLASTIC (51672-1300-5)
51672-1300-951672130009400 g in 1 BOTTLE, PLASTIC (51672-1300-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8bb09bb3-5bbc-489d-96c1-ae97cb58381e

  • NADAC price for package 51672130005

    GET /v1/drugs/nadac/51672130005

  • NADAC price for package 51672130009

    GET /v1/drugs/nadac/51672130009

Use it

Look up 51672-1300 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1300 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-1300. 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.