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Potassium Chloride

NDC 70771-1600, Potassium Chloride, tablet, extended release, from Zydus Lifesciences Limited.

Product NDC
70771-1600
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210395
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1600 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • POTASSIUM CHLORIDE1500 mg/1
Package NDCNDC-11Package
70771-1600-0707711600001000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1600-0)
70771-1600-170771160001100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1600-1)
70771-1600-570771160005500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1600-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/099c3a36-f460-4191-80e5-0c4153a5c713

Use it

Look up 70771-1600 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1600 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1600. 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.