| Product NDC: | 0069-0109 | 
| Proprietary Name: | Pamidronate Disodium | 
| Non Proprietary Name: | Pamidronate Disodium | 
| Active Ingredient(s): | 9 mg/mL & nbsp; Pamidronate Disodium | 
| Administration Route(s): | INTRAVENOUS | 
| Dosage Form(s): | INJECTION, SOLUTION | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 0069-0109 | 
| Labeler Name: | Pfizer Laboratories Div Pfizer Inc | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | ANDA078520 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20110510 | 
| Package NDC: | 0069-0109-01 | 
| Package Description: | 10 mL in 1 VIAL (0069-0109-01) | 
| NDC Code | 0069-0109-01 | 
| Proprietary Name | Pamidronate Disodium | 
| Package Description | 10 mL in 1 VIAL (0069-0109-01) | 
| Product NDC | 0069-0109 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | Pamidronate Disodium | 
| Dosage Form Name | INJECTION, SOLUTION | 
| Route Name | INTRAVENOUS | 
| Start Marketing Date | 20110510 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Pfizer Laboratories Div Pfizer Inc | 
| Substance Name | PAMIDRONATE DISODIUM | 
| Strength Number | 9 | 
| Strength Unit | mg/mL | 
| Pharmaceutical Classes | Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient] |