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levothyroxine sodium

NDC 68788-7704, levothyroxine sodium, tablet, from Preferred Pharmaceuticals, Inc..

Product NDC
68788-7704
Status
Listed
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA021116
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-7704 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LEVOTHYROXINE SODIUM200 ug/1

Pharmacologic classes

Thyroxine [CS]; l-Thyroxine [EPC]

Package NDCNDC-11Package
68788-7704-36878877040330 TABLET in 1 BOTTLE (68788-7704-3)
68788-7704-96878877040990 TABLET in 1 BOTTLE (68788-7704-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/eb53dc23-8337-497e-b466-192f905563ed

Use it

Look up 68788-7704 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-7704 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-7704. 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.