Product Images Glycopyrrolate

View Photos of Packaging, Labels & Appearance

Product Label Images

The following 10 images provide visual information about the product associated with Glycopyrrolate NDC 0143-9586 by Hikma Pharmaceuticals Usa Inc., such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

chemical structure - glycopyrrolate injection novaplus 1

chemical structure - glycopyrrolate injection   novaplus 1

glycopyrrolate injection novaplus 10

glycopyrrolate injection   novaplus 10

This text provides product identification information including GTIN (Global Trade Item Number), SN (Serial Number), expiration date (EXP), and LOT number. However, without additional context, it is not possible to determine the specific product associated with this information.*

NDC 0143-9587-01 Rx ONLY Glycopyrrolate Injection, USP 1 mL Single Dose Vial 0.2 mg/mL CONTAINS BENZYL ALCOHOL FOR IM OR IV USE - glycopyrrolate injection novaplus 2

NDC 0143-9587-01 Rx ONLY Glycopyrrolate Injection, USP 1 mL Single Dose Vial 0.2 mg/mL CONTAINS BENZYL ALCOHOL FOR IM OR IV USE - glycopyrrolate injection   novaplus 2

This is a description of Glycopyrrolate Injection, USP. It contains 0.2 mg/mL and is for IM or IV use only. The injection is distributed by Hikma and contains Benzyl Alcohol. The product is packaged under the brand name NovaPlus and the National Drug Code (NDC) is 0143-9587-01. The lot number and expiration date are also provided.*

NDC 0143-9587-25 Rx ONLY Glycopyrrolate Injection, USP 25 X 1 mL Single Dose VialS 0.2 mg/mL NOT FOR USE IN NEWBORNS CONTAINS BENZYL ALCOHOL FOR IM OR IV ADMINISTRATION Water for Injection, USP q.s./Benzyl Alcohol, NF (preservative) 0.9%. pH adjusted, when necessary, with hydrochloric acid and/or sodium hydroxide. USUAL DOSAGE: See package insert. Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. - glycopyrrolate injection novaplus 3

NDC 0143-9587-25 Rx ONLY Glycopyrrolate Injection, USP 25 X 1 mL Single Dose VialS 0.2 mg/mL NOT FOR USE IN NEWBORNS CONTAINS BENZYL ALCOHOL FOR IM OR IV ADMINISTRATION Water for Injection, USP q.s./Benzyl Alcohol, NF (preservative) 0.9%. pH adjusted, when necessary, with hydrochloric acid and/or sodium hydroxide. USUAL DOSAGE: See package insert. Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. - glycopyrrolate injection   novaplus 3

This is a description of the medication Glycopyrrolate Injection, USP. It comes in single dose vials with a volume of 251mL and dosage of 0.2mg/m. It should not be used on newborns and contains Benzyl Alcohol. The medication is meant for IM or IV use and consists of Water for Injection and Benzyl Alcohol with an adjusted pH using hydrochloric acid and/or sodium hydroxide. The usual dosage is indicated on the package and it should be stored at temperatures between 20-25°C. The product is manufactured by IO ARAAGELTEA PORTUGL 54, and labeled as novaplus™+.*

NDC 0143-9586-01 Rx ONLY Glycopyrrolate Injection, USP 2 mL Single Dose Vial 0.4 mg/2 mL (0.2 mg/mL) CONTAINS BENZYL ALCOHOL FOR IM OR IV USE - glycopyrrolate injection novaplus 4

NDC 0143-9586-01 Rx ONLY Glycopyrrolate Injection, USP 2 mL Single Dose Vial 0.4 mg/2 mL (0.2 mg/mL) CONTAINS BENZYL ALCOHOL FOR IM OR IV USE - glycopyrrolate injection   novaplus 4

This is a description of a medication called Glycopyrrolate. It is only available with a prescription (Rx ONLY) and is administered via injection (IM or IV). The medication comes in a 2 mL single dose vial containing 0.4 mg per 2 mL (0.2 mg/mL) and contains Benzyl Alcohol. The manufacturer is Hikma and it is distributed under the name "novaplus". The lot and expiration information are unavailable.*

NDC 0143-9586-25 Rx ONLY Glycopyrrolate Injection, USP 25 x 2 mL Single Dose Vials 0.4 mg/2 mL (0.2 mg/mL) NOT FOR USE IN NEWBORNS CONTAINS BENZYL ALCOHOL FOR IM OR IV ADMINISTRATION Water for Injection, USP q.s./Benzyl Alcohol, NF (preservative) 0.9%. pH adjusted, when necessary, with hydrochloric acid and/or sodium hydroxide. USUAL DOSAGE: See package insert. Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. - glycopyrrolate injection novaplus 5

NDC 0143-9586-25 Rx ONLY Glycopyrrolate Injection, USP 25 x 2 mL Single Dose Vials 0.4 mg/2 mL (0.2 mg/mL) NOT FOR USE IN NEWBORNS CONTAINS BENZYL ALCOHOL FOR IM OR IV ADMINISTRATION Water for Injection, USP q.s./Benzyl Alcohol, NF (preservative) 0.9%. pH adjusted, when necessary, with hydrochloric acid and/or sodium hydroxide. USUAL DOSAGE: See package insert. Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. - glycopyrrolate injection   novaplus 5

This is a description of Glycopyrrolate injection, which comes in a package of 25 single-dose 2 mL vials, with each vial containing 0.4 mg of the solution. The injection contains Benzyl Alcohol and is for Intramuscular or Intravenous use only and is not suitable for newborns. The usual dosage of the injection is mentioned on the package insert. It should be stored at 20°C to 25°C, and it is imported and distributed by a company called NovaPlus.*

NDC 0143-9585-01 Rx ONLY Glycopyrrolate Injection, USP 5 mL Multiple Dose Vial 1 mg/5 mL (0.2 mg/mL) NOT FOR USE IN NEWBORNS CONTAINS BENZYL ALCOHOL FOR IM OR IV ADMINISTRATION Water for Injection, USP q.s./ Benzyl Alcohol, NF (preserva- tive) 0.9%. pH adjusted, when necessary, with hydrochloric acid and/or sodium hydroxide. USUAL DOSAGE: See package insert. Store at 20° to 25°C (68° to 77°F). - glycopyrrolate injection novaplus 6

NDC 0143-9585-01 Rx ONLY Glycopyrrolate Injection, USP 5 mL Multiple Dose Vial 1 mg/5 mL (0.2 mg/mL) NOT FOR USE IN NEWBORNS CONTAINS BENZYL ALCOHOL FOR IM OR IV ADMINISTRATION Water for Injection, USP q.s./ Benzyl Alcohol, NF (preserva- tive) 0.9%. pH adjusted, when necessary, with hydrochloric acid and/or sodium hydroxide. USUAL DOSAGE: See package insert. Store at 20° to 25°C (68° to 77°F). - glycopyrrolate injection   novaplus 6

This appears to be a label for a medication called Glycopyrrolate Injection, with a concentration of 0.2 mg/mL, and packaged in a single-dose vial under the brand name novaplus®. The label also includes a lot number and expiration date.*

NDC 0143-9585-25 Rx ONLY Glycopyrrolate Injection, USP 25 x 5 mL Multiple Dose Vials 1 mg/5 mL (0.2 mg/mL) NOT FOR USE IN NEWBORNS CONTAINS BENZYL ALCOHOL FOR IM OR IV ADMINISTRATION Water for Injection, USP q.s./Benzyl Alcohol, NF (preservative) 0.9%. pH adjusted, when necessary, with hydrochloric acid and/or sodium hydroxide. USUAL DOSAGE: See package insert. Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. - glycopyrrolate injection novaplus 7

NDC 0143-9585-25 Rx ONLY Glycopyrrolate Injection, USP 25 x 5 mL Multiple Dose Vials 1 mg/5 mL (0.2 mg/mL) NOT FOR USE IN NEWBORNS CONTAINS BENZYL ALCOHOL FOR IM OR IV ADMINISTRATION Water for Injection, USP q.s./Benzyl Alcohol, NF (preservative) 0.9%. pH adjusted, when necessary, with hydrochloric acid and/or sodium hydroxide. USUAL DOSAGE: See package insert. Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. - glycopyrrolate injection   novaplus 7

Glycopyrrolate is a prescription injection available in 25 x 5 mL vials with a strength of 1mg per 5 mL. It is not recommended for newborns and contains Benzyl Alcohol. The injection is for intramuscular or intravenous use and should be stored between 20°C to 25°C. The pH is adjusted as necessary with hydrochloric acid and/or sodium hydroxide. The usual dosage is provided in the package insert. The product is manufactured and distributed by KA FARVACEUTIGA in Portugal and the NDC (National Drug Code) is 0143-9585-25.*

NDC 0143-9584-01 Rx ONLY Glycopyrrolate Injection, USP 20 mL Multiple Dose Vial 4 mg/20 mL (0.2 mg/mL) NOT FOR USE IN NEWBORNS CONTAINS BENZYL ALCOHOL FOR IM OR IV ADMINISTRATION Water for Injection, USP q.s./Benzyl Alcohol, NF (preservative) 0.9%. pH adjusted, when necessary, with hydrochloric acid and/or sodium hydroxide. USUAL DOSAGE: See package insert. Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. - glycopyrrolate injection novaplus 8

NDC 0143-9584-01 Rx ONLY Glycopyrrolate Injection, USP 20 mL Multiple Dose Vial 4 mg/20 mL (0.2 mg/mL) NOT FOR USE IN NEWBORNS CONTAINS BENZYL ALCOHOL FOR IM OR IV ADMINISTRATION Water for Injection, USP q.s./Benzyl Alcohol, NF (preservative) 0.9%. pH adjusted, when necessary, with hydrochloric acid and/or sodium hydroxide. USUAL DOSAGE: See package insert. Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. - glycopyrrolate injection   novaplus 8

Glycopyrrolate Injection is a medication used for intramuscular or intravenous administration. It is available in a 20 mL multiple dose vial and contains 4 mg per 20 mL. However, it is not recommended for use in newborns and contains benzyl alcohol. The solution is a mixture of water for injection and benzoic acid. The pH and ionic strength can be adjusted if necessary using citric acid and/or sodium hydroxide. It is recommended to check the dosage instructions on the package insert. The medication should be stored at a temperature of 20–25°C (68–77°F).*

NDC 0143-9584-10 Rx ONLY Glycopyrrolate Injection, USP 10 x 20 mL Multiple Dose Vials 4 mg/20 mL (0.2 mg/mL) NOT FOR USE IN NEWBORNS CONTAINS BENZYL ALCOHOL FOR IM OR IV ADMINISTRATION Water for Injection, USP q.s./Benzyl Alcohol, NF (preservative) 0.9%. pH adjusted, when necessary, with hydrochloric acid and/or sodium hydroxide. USUAL DOSAGE: See package insert. Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. - glycopyrrolate injection novaplus 9

NDC 0143-9584-10 Rx ONLY Glycopyrrolate Injection, USP 10 x 20 mL Multiple Dose Vials 4 mg/20 mL (0.2 mg/mL) NOT FOR USE IN NEWBORNS CONTAINS BENZYL ALCOHOL FOR IM OR IV ADMINISTRATION Water for Injection, USP q.s./Benzyl Alcohol, NF (preservative) 0.9%. pH adjusted, when necessary, with hydrochloric acid and/or sodium hydroxide. USUAL DOSAGE: See package insert. Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. - glycopyrrolate injection   novaplus 9

This text provides information about a medication called Glycopyrrolate. The medication is available in injections and comes in a pack of 10 x 20 mL Multiple Dose vials, with each vial containing 4 mg per 20 mL (0.2 mg/m). It is not for use in newborns and contains Benzyl Alcohol. The medication can be administered intramuscularly or intravenously. The packaging has instructions on how to open it, and it contains Water for injection and Benzyl Alcohol as a preservative. The medication should be stored at 20° to 25°C (68° o 77°F) [See USP Controlled Room Temperature].*

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.