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IBUPROFEN

NDC 68210-0200, IBUPROFEN, capsule, liquid filled, from SPIRIT PHARMACEUTICALS,LLC.

Product NDC
68210-0200
Status
Listed
Labeler
SPIRIT PHARMACEUTICALS,LLC
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA079205
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68210-0200 \
  -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
68210-0200-1682100200011 BOTTLE in 1 CARTON (68210-0200-1) / 10 CAPSULE, LIQUID FILLED 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 68210-0200 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68210-0200 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68210-0200. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.