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Theophylline

NDC 68462-721 · Glenmark Pharmaceuticals Inc., USA

Generic nameTheophylline
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)THEOPHYLLINE ANHYDROUS
Strength300 mg/1
Pharmacologic classMethylxanthine [EPC], Xanthines [CS]
Marketing categoryANDA

Packages

68462-721-01 — 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-721-01)

68462-721-05 — 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-721-05)

68462-721-10 — 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-721-10)

68462-721-30 — 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-721-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

60219-2045 — theophylline, 60219-2046 — theophylline, 62135-457 — Theophylline, 62135-556 — Theophylline, 62332-025 — Theophylline, 62332-026 — Theophylline, 64380-243 — Theophylline, 64380-244 — Theophylline, 68462-356 — Theophylline, 68462-380 — Theophylline, 68462-722 — Theophylline, 68999-556 — Theophylline, 69367-414 — Theophylline Anhydrous, 69367-415 — Theophylline Anhydrous, 69452-267 — Theophylline, 70771-1782 — Theophylline, 70771-1783 — Theophylline, 71335-2909 — Theophylline, 72162-2038 — Theophylline, 72578-173 — 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.