Olinvyk Injection, Solution
Product Images NDC 71308-011

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Olinvyk (NDC 71308-011). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Trevena, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Structural Formula (Olinvyk 1)

Structural Formula (Olinvyk 1)
Chemical structure of the active ingredient in OLINVYK, depicted with rings containing nitrogen, oxygen, sulfur, and carboxylic acid groups, consistent with the molecular composition of the drug.*
FDA Label Image

Figure 1 (Olinvyk 2)

Figure 1 (Olinvyk 2)
A line graph depicting average pain scores over 48 hours for different treatments: placebo, OLINVYK 0.35 mg, OLINVYK 0.5 mg, and morphine. The x-axis represents time in hours, and the y-axis shows average pain score values from 0 to 10. Each treatment group is represented by distinct line styles and markers.*
FDA Label Image

Figure 2 (Olinvyk 3)

Figure 2 (Olinvyk 3)
A line chart depicting average pain scores over 24 hours for different treatments: Placebo, OLINVYK 0.35 mg, OLINVYK 0.5 mg, and Morphine. The x-axis represents time in hours, and the y-axis shows the average pain score. The chart compares pain relief effects of these treatments over time.*
FDA Label Image

1 mg/ml (Vial Label)

1 mg/ml (Vial Label)
Label for OLINVYK (oliceridine) injection showing a concentration of 1 mg/mL. It is a single-dose vial for intravenous use only. The label includes storage instructions, barcodes, the NDC number 71308-011-01, and identifies Trevena, Inc. as the manufacturer.*
FDA Label Image

1 mg/ml (Carton Label)

1 mg/ml (Carton Label)
Carton label for OLINVYK (oliceridine) injection 1 mg/mL by Trevena, Inc. The label indicates the product is for intravenous use only and contains 10 single-dose vials of 1 mg/mL solution. The packaging includes warnings about habit formation and cautions against use by persons for whom it was not prescribed. It displays the NDC number 71308-011-10 and includes storage instructions, barcode, lot, and expiration details.*
FDA Label Image

2 mg/2 mL (Vial Label)

2 mg/2 mL (Vial Label)
The packaging label for OLINVYK (oliceridine) injection, showing strength of 2 mg per 2 mL (1 mg/mL). The label specifies use for intravenous administration and indicates sterile single-dose vial. The labeler is Trevena, Inc. NDC 71308-021-01 is visible along with usage and storage instructions.*
FDA Label Image

2 mg/ 2 mL (Carton Label)

2 mg/ 2 mL (Carton Label)
Carton packaging label for OLINVYK 2 mg/2 mL (1 mg/mL) injection by Trevena, Inc. The label states it is for intravenous use only and includes warnings about habit formation. The carton contains 10 single-dose vials with dosage instructions and storage conditions. Barcodes and tamper-evident tape areas are visible on the design.*
FDA Label Image

30 mg/30 mL (Vial Label)

30 mg/30 mL (Vial Label)
Label for OLINVYK (oliceridine) injection, 30 mg/30 mL (1 mg/mL) in a single-patient-use vial. The label states it is for intravenous use only, specifically PCA use, and to discard unused portions. It is manufactured for Trevena, Inc., with storage instructions and a barcode included.*
FDA Label Image

30 mg/ 30 mL (Carton Label)

30 mg/ 30 mL (Carton Label)
Packaging label for OLINVYK (oliceridine) injection 30 mg/30 mL (1 mg/mL) single-patient-use vials. The carton contains 10 vials of 30 mg/30 mL solution, labeled for intravenous use only and PCA use only. Manufactured by Trevena, Inc., the label includes warnings about habit-forming potential and safe storage instructions.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.