Duramorph Injection
Product Images NDC 0641-6020

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Duramorph (NDC 0641-6020). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa 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.

Product Images & Figures Index

FDA Label Image

Structure (Duramorph 1)

Structure (Duramorph 1)
Chemical structure diagram of morphine sulfate pentahydrate, depicting the molecular arrangement including sulfate and water components associated with the morphine base.*
FDA Label Image

Ndc 0641-6020-01 Preservative-free Duramorph (morphine Sulfate Injection, Usp) Cii 5 mg/10 mL (0.5 mg/ml) 10 mL Ampul Rx Only For Intravenous, Epidural Or Intrathecal Administration-read Package Insert Carefully Each mL Contains Morphine Sulfate 0.5 mg And Sodium Chloride 9 mg In Water For Injection. Ph 2.5-6.5 Protect From Light. Do Not Use If Color Is Darker Than Pale Yellow, If It Is Discolored In Any Other Way Or If It Contains A Precipitate. Do Not Heat-sterilize. (Duramorph 2)

Ndc 0641-6020-01 Preservative-free Duramorph (morphine Sulfate Injection, Usp) Cii 5 mg/10 mL (0.5 mg/ml) 10 mL Ampul Rx Only For Intravenous, Epidural Or Intrathecal Administration-read Package Insert Carefully Each mL Contains Morphine Sulfate 0.5 mg And Sodium Chloride 9 mg In Water For Injection. Ph 2.5-6.5 Protect From Light. Do Not Use If Color Is Darker Than Pale Yellow, If It Is Discolored In Any Other Way Or If It Contains A Precipitate. Do Not Heat-sterilize. (Duramorph 2)
Duramorph (Morphine Sulfate Injection, USP) preservative-free injection label displaying strength 5 mg per 10 mL (0.5 mg/mL). The 10 mL ampul is labeled for intravenous, epidural, or intrathecal use. Manufactured by Hikma Pharmaceuticals USA Inc., the label includes usage instructions, storage warnings, and lot/expiration date sections.*
FDA Label Image

Ndc 0641-6020-10 Rx Only Preservative-free Duramorph (morphine Sulfate Injection, Usp) Cii 5 mg/10 mL (0.5 mg/ml) For Intravenous, Epidural Or Intrathecal Administration 10 X 10 mL Ampuls Each mL Contains Morphine Sulfate 0.5 mg And Sodium Chloride 9 mg In Water For Injection. Ph 2.5-6.5. Usual Dosage And Adminstration: Read Package Insert. Protect From Light: Keep Covered In Carton Until Time Of Use. Store At 20º-25ºc (68º-77ºf), Excursions Permitted To 15º-30ºc (59º-86ºf) [see Usp Controlled Room Temperature]. Do Not Use If Color Is Darker Than Pale Yellow, If It Is Discolored In Any Way Or If It Contains A Precipitate. Contains No Preservative. Discard Any Unused Portion. Do Not Heat-sterilize. To Open Ampuls, Ignore Color Line; Break At Constriction. (Duramorph 3)

Ndc 0641-6020-10 Rx Only Preservative-free Duramorph (morphine Sulfate Injection, Usp) Cii 5 mg/10 mL (0.5 mg/ml) For Intravenous, Epidural Or Intrathecal Administration 10 X 10 mL Ampuls Each mL Contains Morphine Sulfate 0.5 mg And Sodium Chloride 9 mg In Water For Injection. Ph 2.5-6.5. Usual Dosage And Adminstration: Read Package Insert. Protect From Light: Keep Covered In Carton Until Time Of Use. Store At 20º-25ºc (68º-77ºf), Excursions Permitted To 15º-30ºc (59º-86ºf) [see Usp Controlled Room Temperature]. Do Not Use If Color Is Darker Than Pale Yellow, If It Is Discolored In Any Way Or If It Contains A Precipitate. Contains No Preservative. Discard Any Unused Portion. Do Not Heat-sterilize. To Open Ampuls, Ignore Color Line; Break At Constriction. (Duramorph 3)
Duramorph 5 mg per 10 mL (0.5 mg/mL) injection label showing morphine sulfate injection, USP in preservative free form. The label states it is for intravenous, epidural, or intrathecal use, and includes storage instructions and warnings. The labeler is Hikma Pharmaceuticals USA Inc. The package contains 10 x 10 mL ampuls.*
FDA Label Image

Ndc 0641-6019-01 Preservative-free Duramorph (morphine Sulfate Injection, Usp) Cii 10 mg/10 mL (1 mg/ml) 10 mL Ampul Rx Only For Intravenous, Epidural Or Intrathecal Administration-read Package Insert Carefully Each mL Contains Morphine Sulfate 1 mg And Sodium Chloride 9 mg In Water For Injection. Ph 2.5-6.5. Protect From Light. Do Not Use If Color Is Darker Than Pale Yellow, If It Is Discolored In Any Other Way Or If It Contains A Precipitate. Do Not Heat-sterilize. (Duramorph 4)

Ndc 0641-6019-01 Preservative-free Duramorph (morphine Sulfate Injection, Usp) Cii 10 mg/10 mL (1 mg/ml) 10 mL Ampul Rx Only For Intravenous, Epidural Or Intrathecal Administration-read Package Insert Carefully Each mL Contains Morphine Sulfate 1 mg And Sodium Chloride 9 mg In Water For Injection. Ph 2.5-6.5. Protect From Light. Do Not Use If Color Is Darker Than Pale Yellow, If It Is Discolored In Any Other Way Or If It Contains A Precipitate. Do Not Heat-sterilize. (Duramorph 4)
Duramorph Morphine Sulfate Injection USP 10 mg per 10 mL (1 mg/mL) preservative free, 10 mL ampul vial label from Hikma Pharmaceuticals USA Inc. The label indicates use for intravenous, epidural, or intrathecal administration and provides information on contents, storage, and warnings including not to use if discolored or containing precipitate and to protect from light.*
FDA Label Image

Ndc 0641-6019-10 Rx Only Preservative-free Duramorph (morphine Sulfate Injection, Usp) Cii 10 mg/10 mL (1 mg/ml) For Intravenous, Epidural Or Intrathecal Administration 10 X 10 mL Ampuls Each mL Contains Morphine Sulfate 1 mg And Sodium Chloride 9 mg In Water For Injection. Ph 2.5-6.5. Usual Dosage And Administration: Read Package Insert. Protect From Light. Keep Covered In Carton Until Time Of Use. Store At 20º-25ºc (68º-77ºf), Excursion Permitted To 15º-30ºc (59º-86ºf) [ See Usp Controlled Room Temperature]. Do Not Use If Color Is Darker Than Pale Yellow, If It Is Discolored In Any Other Way Or If It Contains A Precipitate. Contains No Perservative. Discard Any Unused Portion. Do Not Heat-sterilize. To Open Ampuls, Ignore Color Line; Break At Constriction. (Duramorph 5)

Ndc 0641-6019-10 Rx Only Preservative-free Duramorph (morphine Sulfate Injection, Usp) Cii 10 mg/10 mL (1 mg/ml) For Intravenous, Epidural Or Intrathecal Administration 10 X 10 mL Ampuls Each mL Contains Morphine Sulfate 1 mg And Sodium Chloride 9 mg In Water For Injection. Ph 2.5-6.5. Usual Dosage And Administration: Read Package Insert. Protect From Light. Keep Covered In Carton Until Time Of Use. Store At 20º-25ºc (68º-77ºf), Excursion Permitted To 15º-30ºc (59º-86ºf) [ See Usp Controlled Room Temperature]. Do Not Use If Color Is Darker Than Pale Yellow, If It Is Discolored In Any Other Way Or If It Contains A Precipitate. Contains No Perservative. Discard Any Unused Portion. Do Not Heat-sterilize. To Open Ampuls, Ignore Color Line; Break At Constriction. (Duramorph 5)
Duramorph 10 mg per 10 mL (1 mg/mL) morphine sulfate injection vial label, preservative-free, for intravenous, epidural, or intrathecal use. The label includes storage instructions, usage warnings, and manufacturer details for Hikma Pharmaceuticals USA Inc. Package contains 10 x 10 mL ampuls.*
FDA Label Image

Duramorph 6

Duramorph 6
Duramorph (morphine sulfate) injection label showing a QR code along with serial number, expiration date, and lot number information in a black and white format.*

* 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.