| Product NDC: | 45567-0415 |
| Proprietary Name: | Pulmolite, Kit for the Preparation of Technetium Tc99m Albumin Aggregated for Injection |
| Non Proprietary Name: | Albumin Aggregated |
| Active Ingredient(s): | 1 mg/10mL & nbsp; Albumin Aggregated |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 45567-0415 |
| Labeler Name: | Pharmalucence, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017776 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19761118 |
| Package NDC: | 45567-0415-1 |
| Package Description: | 5 VIAL in 1 KIT (45567-0415-1) > 10 mL in 1 VIAL |
| NDC Code | 45567-0415-1 |
| Proprietary Name | Pulmolite, Kit for the Preparation of Technetium Tc99m Albumin Aggregated for Injection |
| Package Description | 5 VIAL in 1 KIT (45567-0415-1) > 10 mL in 1 VIAL |
| Product NDC | 45567-0415 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Albumin Aggregated |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19761118 |
| Marketing Category Name | NDA |
| Labeler Name | Pharmalucence, Inc. |
| Substance Name | ALBUMIN AGGREGATED |
| Strength Number | 1 |
| Strength Unit | mg/10mL |
| Pharmaceutical Classes |