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NDC 70692-801, Cetirizine Hydrochloride, tablet, film coated, from Strive Pharmaceuticals Inc..

Product NDC
70692-801
Status
Listed
Labeler
Strive Pharmaceuticals Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA077829
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70692-801 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CETIRIZINE HYDROCHLORIDE10 mg/1

Pharmacologic classes

Histamine H1 Receptor Antagonists [MoA]; Histamine-1 Receptor Antagonist [EPC]

Package NDCNDC-11Package
70692-801-43706920801431 BLISTER PACK in 1 CARTON (70692-801-43) / 14 TABLET, FILM COATED 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 70692-801 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70692-801 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70692-801. 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.