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Ammonium Lactate

NDC 51672-1301, Ammonium Lactate, cream, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-1301
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
CREAM
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075883
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1301 \
  -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
51672-1301-051672130100385 g in 1 BOTTLE, PLASTIC (51672-1301-0)
51672-1301-2516721301021 TUBE in 1 CARTON (51672-1301-2) / 140 g in 1 TUBE
51672-1301-4516721301042 TUBE in 1 CARTON (51672-1301-4) / 140 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9745b6ce-f532-4e80-b6e9-477ab9db4e30

  • NADAC price for package 51672130100

    GET /v1/drugs/nadac/51672130100

  • NADAC price for package 51672130104

    GET /v1/drugs/nadac/51672130104

Use it

Look up 51672-1301 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1301 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-1301. 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.