Product NDC: | 0006-3395 |
Proprietary Name: | AMINOHIPPURATE SODIUM |
Non Proprietary Name: | aminohippurate sodium |
Active Ingredient(s): | 2 g/10mL & nbsp; aminohippurate sodium |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0006-3395 |
Labeler Name: | Merck Sharp & Dohme Corp. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA005619 |
Marketing Category: | NDA |
Start Marketing Date: | 19441230 |
Package NDC: | 0006-3395-11 |
Package Description: | 1 VIAL, SINGLE-DOSE in 1 CARTON (0006-3395-11) > 10 mL in 1 VIAL, SINGLE-DOSE |
NDC Code | 0006-3395-11 |
Proprietary Name | AMINOHIPPURATE SODIUM |
Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (0006-3395-11) > 10 mL in 1 VIAL, SINGLE-DOSE |
Product NDC | 0006-3395 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | aminohippurate sodium |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 19441230 |
Marketing Category Name | NDA |
Labeler Name | Merck Sharp & Dohme Corp. |
Substance Name | AMINOHIPPURATE SODIUM |
Strength Number | 2 |
Strength Unit | g/10mL |
Pharmaceutical Classes |