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Pseudoephedrine Hydrochloride

NDC 63868-143, Pseudoephedrine Hydrochloride, tablet, film coated, extended release, from Chain Drug Marketing Association Inc..

Product NDC
63868-143
Status
Listed
Labeler
Chain Drug Marketing Association Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA077442
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63868-143 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PSEUDOEPHEDRINE HYDROCHLORIDE120 mg/1

Pharmacologic classes

Adrenergic alpha-Agonists [MoA]; alpha-Adrenergic Agonist [EPC]

Package NDCNDC-11Package
63868-143-106386801431010 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (63868-143-10)

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 63868-143 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63868-143 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63868-143. 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.