| Product NDC: | 11704-620 |
| Proprietary Name: | DuoDote |
| Non Proprietary Name: | atropine and pralidoxime chloride |
| Active Ingredient(s): | & nbsp; atropine and pralidoxime chloride |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11704-620 |
| Labeler Name: | Meridian Medical Technologies , Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021983 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20060906 |
| Package NDC: | 11704-620-01 |
| Package Description: | 1 KIT in 1 KIT (11704-620-01) * .7 mL in 1 SYRINGE, GLASS * 2 mL in 1 SYRINGE, GLASS |
| NDC Code | 11704-620-01 |
| Proprietary Name | DuoDote |
| Package Description | 1 KIT in 1 KIT (11704-620-01) * .7 mL in 1 SYRINGE, GLASS * 2 mL in 1 SYRINGE, GLASS |
| Product NDC | 11704-620 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | atropine and pralidoxime chloride |
| Dosage Form Name | KIT |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 20060906 |
| Marketing Category Name | NDA |
| Labeler Name | Meridian Medical Technologies , Inc. |
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