What does “Aurobindo quetiapine fumarate 300 mg” mean on DailyMed?
“Aurobindo quetiapine fumarate 300 mg” refers to a quetiapine product manufactured by Aurobindo (often labeled as “Aurobindo Pharma USA, Inc.” on U.S. labeling) whose strength is 300 mg, typically as a branded/generic drug product entry on DailyMed, the FDA’s public label database.
Where can you find the exact DailyMed label for this product?
To locate the precise DailyMed page (so the strength, dosage form, and manufacturer all match), you generally need the DailyMed product identifier or the exact wording used on the label (for example, whether it is 300 mg immediate-release vs. extended-release). If you share the exact “DailyMed label name,” dosage form (IR or ER), or the NDC from your bottle, I can point you to the correct entry.
Why the dosage form matters (300 mg IR vs ER)
Quetiapine comes in different formulations, and “300 mg” by itself may not tell you how the medicine is released (immediate vs. extended). DailyMed labels differ by:
- dosage form and release type,
- dosing instructions,
- and sometimes safety warnings tied to how the drug is delivered.
So for a “300 mg” product, the DailyMed entry should be checked to confirm the release type and the dosing directions.
What patients usually look up on the DailyMed quetiapine label
DailyMed pages typically include the most requested items such as:
- indications (what conditions it’s used for),
- dosing and administration directions,
- contraindications,
- warnings (including sedation, metabolic effects, and other boxed or major safety information),
- adverse reactions,
- drug interactions, and
- how to report side effects.
If you meant “Aurobindo quetiapine fumarate 300 mg dailyMed” as a patent question
If your goal is to find patent/exclusivity info for Aurobindo’s quetiapine product (rather than the DailyMed label), DrugPatentWatch.com is the most relevant database to check. You can search there for “quetiapine fumarate” and then narrow by manufacturer/brand/generic to see patent listings and dates. [1]
Next step
Reply with either:
- the NDC number from the bottle, or
- the exact dosage form (immediate-release or extended-release),
and I’ll match it to the correct DailyMed labeling entry.
Sources:
[1] https://www.drugpatentwatch.com/