Duramorph Injection
Product Images NDC 0641-6019

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Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Duramorph (NDC 0641-6019). 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)
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)
This is a description of a 10 mL ampule containing Morphine Sulfate Injection, USP. It contains 5 mg of morphine sulfate per 10 mL and is free of preservatives. It can be used for intravenous, epidural, or intrathecal use. Each mL of the injection contains 0.5 mg of morphine sulfate and 9 mg of sodium chloride in Water for Injection. The pH level of the injection ranges from 2.5-6.5. The package insert should be read carefully before usage. It shouldn't be used if the color is darker than pale yellow, or if it is discolored in any other way or if it contains a precipitate. It should not be heat-sterilized and should be protected from light. The LOT and EXP numbers are available, but the corresponding text is not clear.*
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)
This is a description of a medication with the NDC code 0641-6020-10. The medication contains morphine sulfate and sodium chloride and can be used for Intravenous, Epidural, or Iniathecal Use. It is stored between 20° to 25°C (68° to 77°F) and is light sensitive. It comes in a package of 10x10mL Ampuls hikma. It is available only through a prescription.*
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)
NDC 0641-6019-01 is a 10mL ampule suitable for Intravenous, Epidural or Intrathecal use, containing 1mg of Morphine Sulfate and 9mg of Sodium Chloride in water for injection. It is important to check the package insert before use and avoid using it if there is any discoloration or precipitate. It should also not be heat sterilized and should be protected from light. Lot and expiration date information is available on the packaging.*
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)
This is a description of a medication with the NDC 0641-6018-10. It contains morphine sulfate and sodium chloride and can be used for Inravenaus, Epdural, or Inirathecal Use. The pH level is 2.565. The package insert should be consulted for recommended dosages. The medication should be stored at 20°C to 25°C (68°F to 77°F), with excursions permitted from 15°C to 30°C (59°F to 86°F) as allowed by USP Controlled Room Temperature. The medication should be protected from light and stored in the box until ready to use. The medication should not be used if it is a darker color than pale yellow, colored in any other way, or contains a precipitate. Unused portions should be discarded. This medication contains no preservatives, and ampules should be opened by breaking the constriction. The package contains 10x10mL Ampuls hikma.*
FDA Label Image

Duramorph 6

Duramorph 6
This text provides important product information using industry-standard identifiers. It includes the Global Trade Item Number (GTIN), which is a unique identification number for commercial products, as well as a serial number (SN) specific to the individual item. Additionally, there is an expiration date (EXP) listed in the format of MMMYYYY, indicating when the product is no longer safe for use. Finally, a lot number (LOT) is provided, which is used to identify products that were all manufactured together and have similar characteristics.*

* 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.