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Doxycycline

NDC 0527-1535, Doxycycline, tablet, film coated, from Lannett Company, Inc..

Product NDC
0527-1535
Status
Listed
Labeler
Lannett Company, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA065285
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0527-1535 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DOXYCYCLINE75 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
0527-1535-0100527153501100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1535-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4999bbd9-44ed-4749-9730-be2337bdf490

Use it

Look up 0527-1535 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0527-1535 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0527-1535. 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.