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Ibuprofen

NDC 68210-8100, Ibuprofen, tablet, film coated, from Spirit Pharmaceutical LLC.

Product NDC
68210-8100
Status
Listed
Labeler
Spirit Pharmaceutical LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA079174
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68210-8100 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • IBUPROFEN200 mg/1

Pharmacologic classes

Anti-Inflammatory Agents, Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Nonsteroidal Anti-inflammatory Drug [EPC]

Package NDCNDC-11Package
68210-8100-2682108100021 BOTTLE in 1 CARTON (68210-8100-2) / 25 TABLET, FILM COATED in 1 BOTTLE
68210-8100-3682108100031 BOTTLE in 1 CARTON (68210-8100-3) / 30 TABLET, FILM COATED in 1 BOTTLE
68210-8100-5682108100051 BOTTLE in 1 CARTON (68210-8100-5) / 50 TABLET, FILM COATED in 1 BOTTLE

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 68210-8100 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68210-8100 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68210-8100. 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.