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Loperamide Hydrochloride and Simethicone

NDC 79903-223, Loperamide Hydrochloride and Simethicone, tablet, from WALMART INC..

Product NDC
79903-223
Status
Listed
Labeler
WALMART INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA211059
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/79903-223 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LOPERAMIDE HYDROCHLORIDE2 mg/1
  • DIMETHICONE125 mg/1

Pharmacologic classes

Opioid Agonist [EPC]; Opioid Agonists [MoA]; Skin Barrier Activity [PE]

Package NDCNDC-11Package
79903-223-12799030223122 BLISTER PACK in 1 CARTON (79903-223-12) / 6 TABLET in 1 BLISTER PACK
79903-223-24799030223244 BLISTER PACK in 1 CARTON (79903-223-24) / 6 TABLET in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 79903-223 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/79903-223 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 79903-223. 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.