Humatrope 36 UI 12 mg Lilly EP

Humatrope 36 UI 12 mg Lilly EP is presented here as a Lilly-labelled product reference with the stated strength shown in the listing title. The available information identifies the brand and manufacturer as Lilly and notes that this is an expired product. Where identification matters, the stated strength, brand naming and any packaging details should be checked together rather than relying on one element alone.

The existing product information also notes an expiry date of 2018.05 and states that the item was stored in a cold room. Because this listing is described as expired, the main value of the page is clear specification and packaging identification. If comparing different listings, check that the product name, stated 36 UI / 12 mg presentation and Lilly branding appear consistently across the label, outer packaging and any printed batch or reference information visible on the pack.

Product Identification and Comparison

When reviewing this listing, focus on the exact naming format, the stated strength and the manufacturer details. Products in this area may appear in different strengths or pack formats, so it is important to distinguish the 36 UI / 12 mg presentation from other similarly named references. For brand verification, Lilly naming should match the packaging and printed product information. You can also view other Lilly listings for comparison of brand presentation and labelling style.

Technical Information

Handling and Verification Notes

Retain the packaging for verification. Check that the printed product name, brand and stated strength are legible and consistent across all visible packaging elements. Store according to the information printed on the original packaging. As this listing is identified as expired, any assessment should remain limited to product reference, packaging review and specification checking.

Frequently Asked Questions

What does EP mean in this listing?

In this context, EP is presented alongside the product name and the listing description identifies it as an expired product.

How should the 36 UI and 12 mg figures be interpreted?

They are the stated strength markers shown in the listing title. For accuracy, these figures should be matched against the printed packaging information.

What is the most important point to verify on the packaging?

The clearest checks are the product name, Lilly branding, stated 36 UI / 12 mg presentation and any printed model or batch-related information visible on the pack.

Is any storage information provided?

The listing states that the product was stored in a cold room. For ongoing handling, follow the information printed on the original packaging.

Why is the expiry date relevant here?

The listing specifically notes expiry information, so it is a key part of identifying the item correctly and distinguishing it from non-expired references.

How can this listing be compared with similar products?

Compare the exact naming format, stated strength, manufacturer details and packaging presentation, as similar products may appear in different strengths or pack formats.