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Ibuprofen and Pseudoephedrine hydrochloride

NDC 51660-423, ibuprofen and pseudoephedrine hydrochloride, tablet, sugar coated, from Ohm Laboratories Inc..

Product NDC
51660-423
Status
Listed
Labeler
Ohm Laboratories Inc.
Dosage form
TABLET, SUGAR COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA074567
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51660-423 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • IBUPROFEN200 mg/1
  • PSEUDOEPHEDRINE HYDROCHLORIDE30 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
51660-423-215166004232120 TABLET, SUGAR COATED in 1 BLISTER PACK (51660-423-21)
51660-423-415166004234140 TABLET, SUGAR COATED in 1 BLISTER PACK (51660-423-41)

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 51660-423 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51660-423 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.