| Product NDC: | 65174-288 |
| Proprietary Name: | Pentetic Acid |
| Non Proprietary Name: | Pentetic Acid |
| Active Ingredient(s): | 20 mg/1 & nbsp; Pentetic Acid |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 65174-288 |
| Labeler Name: | Jubilant DraxImage Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018511 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19891229 |
| Package NDC: | 65174-288-05 |
| Package Description: | 5 INJECTION in 1 KIT (65174-288-05) |
| NDC Code | 65174-288-05 |
| Proprietary Name | Pentetic Acid |
| Package Description | 5 INJECTION in 1 KIT (65174-288-05) |
| Product NDC | 65174-288 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Pentetic Acid |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19891229 |
| Marketing Category Name | NDA |
| Labeler Name | Jubilant DraxImage Inc. |
| Substance Name | PENTETIC ACID |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Lead Chelating Activity [MoA],Lead Chelator [EPC] |