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Doxycycline

NDC 63304-130, Doxycycline, tablet, film coated, from Sun Pharmaceutical Industries Inc..

Product NDC
63304-130
Status
Listed
Labeler
Sun Pharmaceutical Industries Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA065356
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63304-130 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DOXYCYCLINE50 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
63304-130-10633040130101000 TABLET, FILM COATED in 1 BOTTLE (63304-130-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8224b9c5-5c4b-4dda-bc58-47b6604c2884

Use it

Look up 63304-130 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63304-130 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63304-130. 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.