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Potassium chloride

NDC 33342-417, Potassium chloride, tablet, film coated, extended release, from Macleods Pharmaceuticals Limited.

Product NDC
33342-417
Status
Listed
Labeler
Macleods Pharmaceuticals Limited
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212987
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/33342-417 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • POTASSIUM CHLORIDE600 mg/1

Pharmacologic classes

Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Potassium Compounds [CS]; Potassium Salt [EPC]

Package NDCNDC-11Package
33342-417-1133342041711100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (33342-417-11)
33342-417-123334204171210 BLISTER PACK in 1 CARTON (33342-417-12) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
33342-417-1533342041715500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (33342-417-15)
33342-417-343334204173410 BLISTER PACK in 1 CARTON (33342-417-34) / 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e0562a05-4359-4256-87e3-fcde65a008cd

Use it

Look up 33342-417 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/33342-417 \
  -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.