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Rough (Redroot) Pigweed
Rough (Redroot) Pigweed - 49288-0408-3 - (Rough (Redroot) Pigweed)
Drug Information of Rough (Redroot) Pigweed
| Product NDC: | 49288-0408 |
| Proprietary Name: | Rough (Redroot) Pigweed |
| Non Proprietary Name: | Rough (Redroot) Pigweed |
| Active Ingredient(s): | .1 g/mL & nbsp; Rough (Redroot) Pigweed |
| Administration Route(s): | INTRADERMAL; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Rough (Redroot) Pigweed
| Product NDC: | 49288-0408 |
| Labeler Name: | Antigen Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA102223 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19920413 |
Package Information of Rough (Redroot) Pigweed
| Package NDC: | 49288-0408-3 |
| Package Description: | 10 mL in 1 VIAL, MULTI-DOSE (49288-0408-3) |
NDC Information of Rough (Redroot) Pigweed
| NDC Code | 49288-0408-3 |
| Proprietary Name | Rough (Redroot) Pigweed |
| Package Description | 10 mL in 1 VIAL, MULTI-DOSE (49288-0408-3) |
| Product NDC | 49288-0408 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Rough (Redroot) Pigweed |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRADERMAL; SUBCUTANEOUS |
| Start Marketing Date | 19920413 |
| Marketing Category Name | BLA |
| Labeler Name | Antigen Laboratories, Inc. |
| Substance Name | AMARANTHUS RETROFLEXUS POLLEN |
| Strength Number | .1 |
| Strength Unit | g/mL |
| Pharmaceutical Classes | Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient] |
