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Hyoscyamine Sulfate

NDC 16477-738, Hyoscyamine Sulfate, tablet, extended release, from Laser Pharmaceuticals, LLC.

Product NDC
16477-738
Status
Listed
Labeler
Laser Pharmaceuticals, LLC
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/16477-738 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYOSCYAMINE SULFATE.375 mg/1
Package NDCNDC-11Package
16477-738-0116477073801100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16477-738-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b12f856f-7157-4aee-bf73-1fdcb4834ffc

Use it

Look up 16477-738 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16477-738 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16477-738. 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.