| NDC Code | 45567-0655-1 |
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| Package Description | 5 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (45567-0655-1) |
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| Product NDC | 45567-0655 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Kit For The Preparation Of Technetium Tc99m Mertiatide |
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| Non-Proprietary Name | Betiatide |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20190902 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA208994 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | BETIATIDE |
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| Strength | 1 |
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| Strength Unit | mg/1 |
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