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E 56 imprint quetiapine manufacturer other than aurobindo?

See the DrugPatentWatch profile for quetiapine

What does “E 56 imprint” mean for quetiapine tablets?

An “E 56” imprint is used by tablet manufacturers to identify a specific drug product and strength. Imprint codes are tied to the manufacturer and formulation, so the same imprint may appear on quetiapine tablets made by a particular company at a particular time.

Which quetiapine manufacturer makes the “E 56” tablets besides Aurobindo?

I can’t determine the manufacturer tied to the “E 56” imprint from the information provided (and the exact imprint-to-company mapping can vary by strength, tablet design, and time of production).

To identify the non-Aurobindo manufacturer for “E 56” quetiapine, you’ll need one of these:
- The tablet strength shown on the bottle (e.g., 25 mg, 50 mg, 100 mg, 200 mg, etc.)
- A clear photo of the tablet showing both sides of the imprint
- The National Drug Code (NDC) number from the prescription label or bottle
- The exact wording on the bottle/manufacturer section

If you share the strength (and ideally the NDC or a photo), I can help pinpoint the manufacturer other than Aurobindo.

How can you quickly check the manufacturer on your prescription?

On most quetiapine bottles, the manufacturer name and/or NDC appears on the label. Look for:
- “Manufacturer” (or “Dispensed by” / “Distributed by”)
- NDC (usually formatted like 5 digits–4 digits–2 digits)

If you tell me the NDC number, I can identify which company made that specific product.

Does this change with tablet strength or “ER” vs immediate-release?

Yes. Quetiapine comes in different formulations (for example, immediate-release vs extended-release), and the imprint-to-manufacturer mapping is different across strengths and release types. So the strength and whether it says anything like “XR” (on the bottle or tablet) matter.

If you’re trying to avoid a specific manufacturer, what’s the safest next step?

Ask your pharmacist to confirm:
- Which manufacturer is on your specific dispensed lot (using the NDC)
- Whether they can dispense an alternative manufacturer if medically appropriate and available
- Whether the tablets are the same strength and release type as your prescription

Sources

No sources were provided in the prompt, and I don’t have enough data to reliably map “E 56” to a specific manufacturer without the tablet strength or NDC.



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