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Loperamide hydrochloride and Simethicone

NDC 69452-210, loperamide hydrochloride and simethicone, tablet, from Bionpharma Inc..

Product NDC
69452-210
Status
Listed
Labeler
Bionpharma Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA213484
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69452-210 \
  -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
69452-210-04694520210041 BLISTER PACK in 1 CARTON (69452-210-04) / 6 TABLET in 1 BLISTER PACK
69452-210-12694520210124 BLISTER PACK in 1 CARTON (69452-210-12) / 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 69452-210 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69452-210 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69452-210. 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.