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Theophylline

NDC 17856-0038 · ATLANTIC BIOLOGICALS CORP.

Generic nameTheophylline
Dosage formSOLUTION
RouteORAL
Active ingredient(s)THEOPHYLLINE ANHYDROUS
Strength80 mg/15mL
Pharmacologic classMethylxanthine [EPC], Xanthines [CS]
Marketing categoryANDA

Packages

17856-0038-1 — 50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0038-1) / 15 mL in 1 CUP, UNIT-DOSE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

23155-741 — Theophylline, 23155-742 — Theophylline, 27241-272 — Theophylline, 27241-273 — Theophylline, 27808-033 — Theophylline, 31722-077 — Theophylline, 31722-078 — Theophylline, 42291-922 — Theophylline, 46708-025 — Theophylline, 46708-026 — Theophylline, 51407-318 — Theophylline, 51407-319 — Theophylline, 52244-100 — theophylline anhydrous, 52244-200 — theophylline anhydrous, 52244-300 — theophylline anhydrous, 52244-400 — theophylline anhydrous, 60219-2045 — theophylline, 60219-2046 — theophylline, 62135-457 — Theophylline, 62135-556 — Theophylline, +22 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.