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
0121-4820_895f63e5-665b-4227-8e44-6971ba5ce294
Product NDC
0121-4820
Form
SOLUTION
Composition / generic term
THEOPHYLLINE
Labeler
PAI Holdings, LLC dba PAI Pharma
Marketing category
ANDA
Marketing start / end (source format)
20161216
Source listing expiry
20261231

Source-listed ingredients

  • THEOPHYLLINE — 80 mg/15mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 4 TRAY in 1 CASE (0121-4820-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (0121-4820-15) · 0121-4820-40

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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