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NDC 24208-601, Ketotifen Fumarate, solution/ drops, from Bausch & Lomb Incorporated.

Product NDC
24208-601
Status
Listed
Labeler
Bausch & Lomb Incorporated
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Product type
HUMAN OTC DRUG
Marketing category
NDA
Application
NDA021996
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/24208-601 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • KETOTIFEN FUMARATE.25 mg/mL

Pharmacologic classes

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

Package NDCNDC-11Package
24208-601-05242080601051 BOTTLE, DROPPER in 1 CARTON (24208-601-05) / 5 mL in 1 BOTTLE, DROPPER
24208-601-10242080601101 BOTTLE, DROPPER in 1 CARTON (24208-601-10) / 10 mL in 1 BOTTLE, DROPPER
24208-601-90242080601902 BOTTLE, DROPPER in 1 CARTON (24208-601-90) / 10 mL in 1 BOTTLE, DROPPER

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 24208-601 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/24208-601 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 24208-601. 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.