United States · FDA National Drug Code directory

THEOPHYLLINE

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
69315-227_a7dacdee-6f6b-4b85-b051-7779258a6971
Product NDC
69315-227
Form
TABLET, EXTENDED RELEASE
Composition / generic term
THEOPHYLLINE
Labeler
Leading Pharma, LLC
Marketing category
ANDA
Marketing start / end (source format)
20230515
Source listing expiry
20261231

Source-listed ingredients

  • THEOPHYLLINE — 450 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69315-227-01) · 69315-227-01

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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