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Doxycycline Hyclate

NDC 69668-515, DOXYCYCLINE HYCLATE, tablet, delayed release, from Sonoma Pharmaceuticals, Inc..

Product NDC
69668-515
Status
Listed
Labeler
Sonoma Pharmaceuticals, Inc.
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207494
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69668-515 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DOXYCYCLINE HYCLATE150 mg/1

Pharmacologic classes

Tetracycline-class Drug [EPC]; Tetracyclines [CS]

Package NDCNDC-11Package
69668-515-306966805153030 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (69668-515-30)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4fa26176-a730-48ed-9659-e2f64212f418

Use it

Look up 69668-515 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69668-515 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69668-515. 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.