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GLYCOPYRROLATE
GLYCOPYRROLATE - 54868-0765-0 - (glycopyrrolate)
Drug Information of GLYCOPYRROLATE
| Product NDC: | 54868-0765 |
| Proprietary Name: | GLYCOPYRROLATE |
| Non Proprietary Name: | glycopyrrolate |
| Active Ingredient(s): | .2 mg/mL & nbsp; glycopyrrolate |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GLYCOPYRROLATE
| Product NDC: | 54868-0765 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017558 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110506 |
Package Information of GLYCOPYRROLATE
| Package NDC: | 54868-0765-0 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 PACKAGE (54868-0765-0) > 1 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of GLYCOPYRROLATE
| NDC Code | 54868-0765-0 |
| Proprietary Name | GLYCOPYRROLATE |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 PACKAGE (54868-0765-0) > 1 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 54868-0765 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | glycopyrrolate |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20110506 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | GLYCOPYRROLATE |
| Strength Number | .2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
