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PITOLISANT

NDC 70748-387, pitolisant, tablet, film coated, from Lupin Pharmaceuticals, Inc..

Product NDC
70748-387
Status
Listed
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218846
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70748-387 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PITOLISANT HYDROCHLORIDE17.8 mg/1

Pharmacologic classes

Cytochrome P450 3A4 Inducers [MoA]; Histamine H3 Receptor Antagonists [MoA]; Histamine H3 Receptor Inverse Agonists [MoA]; Histamine-3 Receptor Antagonist/Inverse Agonist [EPC]

Package NDCNDC-11Package
70748-387-01707480387011 BOTTLE in 1 CARTON (70748-387-01) / 30 TABLET, FILM COATED in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6fb94d86-5154-4b69-8470-d1145d426312

Use it

Look up 70748-387 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70748-387 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70748-387. 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.