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PRE-PEN
PRE-PEN - 49471-001-05 - (benzylpenicilloyl polylysine)
Drug Information of PRE-PEN
| Product NDC: | 49471-001 |
| Proprietary Name: | PRE-PEN |
| Non Proprietary Name: | benzylpenicilloyl polylysine |
| Active Ingredient(s): | 60 umol/.25mL & nbsp; benzylpenicilloyl polylysine |
| Administration Route(s): | INTRADERMAL; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PRE-PEN
| Product NDC: | 49471-001 |
| Labeler Name: | AllerQuest LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050114 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19740725 |
Package Information of PRE-PEN
| Package NDC: | 49471-001-05 |
| Package Description: | 5 AMPULE in 1 CARTON (49471-001-05) > .25 mL in 1 AMPULE |
NDC Information of PRE-PEN
| NDC Code | 49471-001-05 |
| Proprietary Name | PRE-PEN |
| Package Description | 5 AMPULE in 1 CARTON (49471-001-05) > .25 mL in 1 AMPULE |
| Product NDC | 49471-001 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | benzylpenicilloyl polylysine |
| Dosage Form Name | INJECTION |
| Route Name | INTRADERMAL; SUBCUTANEOUS |
| Start Marketing Date | 19740725 |
| Marketing Category Name | NDA |
| Labeler Name | AllerQuest LLC |
| Substance Name | BENZYLPENICILLOYL POLYLYSINE |
| Strength Number | 60 |
| Strength Unit | umol/.25mL |
| Pharmaceutical Classes |
