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BONINE MAX

NDC 65197-520, meclizine hydrochloride, tablet, chewable, from WellSpring Pharmaceutical Corporation.

Product NDC
65197-520
Status
Listed
Labeler
WellSpring Pharmaceutical Corporation
Dosage form
TABLET, CHEWABLE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
M009
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65197-520 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MECLIZINE HYDROCHLORIDE50 mg/1

Pharmacologic classes

Antiemetic [EPC]; Emesis Suppression [PE]

Package NDCNDC-11Package
65197-520-16651970520162 BLISTER PACK in 1 BOX (65197-520-16) / 8 TABLET, CHEWABLE in 1 BLISTER PACK
65197-520-17651970520172 BLISTER PACK in 1 BOX (65197-520-17) / 8 TABLET, CHEWABLE 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 65197-520 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65197-520 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65197-520. 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.