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What the FDA labels say about taking them together

Carbamazepine and erlotinib

Erlotinib's FDA label of June 10, 2024 names carbamazepine in its drug interactions section; the carbamazepine labels PlainMeds reads (3) do not name erlotinib. The erlotinib label: “Increase the erlotinib dosage if co-administration with CYP3A4 inducers is unavoidable.”

Check it at the source: the carbamazepine FDA label on DailyMed (effective August 20, 2026, Novartis Pharmaceuticals Corporation); the erlotinib FDA label on DailyMed (effective June 10, 2024, Alembic Pharmaceuticals Limited).

What does the carbamazepine label say about erlotinib?

Carbamazepine's label (effective August 20, 2026) and its 2 other brand-application labels do not name erlotinib in these sections. A label lists what its studies and reports found; it is not a complete list.

Source: FDA drug label (Tegretol), Novartis Pharmaceuticals Corporation, effective August 20, 2026 (SPL set 8d409411-aa9f-4f3a-a52c-fbcb0c3ec053), via openFDA; the full label on DailyMed

What does the erlotinib label say about carbamazepine?

Erlotinib label, drug interactions

Increase the erlotinib dosage if co-administration with CYP3A4 inducers (e.g., carbamazepine, phenytoin, rifampin, rifabutin, rifapentine, phenobarbital and St. John's wort) is unavoidable [see Dosage and Administration (2.4)].

Source: FDA drug label (ERLOTINIB HYDROCHLORIDE), Alembic Pharmaceuticals Limited, effective June 10, 2024 (SPL set ab6f3cb3-34a8-4492-a5d7-fb6b055a2d6b), via openFDA; the full label on DailyMed

These are the labels' own sentences. PlainMeds does not grade interactions; a pharmacist or prescriber can say what they mean for one person's medicines.

Both medicines on the record

42Carbamazepine generic labelers
10Erlotinib generic labelers
CarbamazepineErlotinib
Labeled forBipolar disorder, Seizures and epilepsyLung cancer
Boxed warningYesNo
Pharmacy cost (NADAC)$0.119 per tablet 200 mg tabletn/a
Shortage nowA presentation being discontinuedNo current entry

Source: FDA NDC Directory, CMS NADAC of October 7, 2026 and the FDA Drug Shortage Database (FDA files October 8, 2026)

What next?