| Product NDC: | 51808-209 |
| Proprietary Name: | Thyrotropin Releasing Hormone |
| Non Proprietary Name: | Thyrotropin Releasing Hormone |
| Active Ingredient(s): | 500 ug/mL & nbsp; Thyrotropin Releasing Hormone |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 51808-209 |
| Labeler Name: | AnazaoHealth Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120619 |
| Package NDC: | 51808-209-01 |
| Package Description: | 1 mL in 1 VIAL (51808-209-01) |
| NDC Code | 51808-209-01 |
| Proprietary Name | Thyrotropin Releasing Hormone |
| Package Description | 1 mL in 1 VIAL (51808-209-01) |
| Product NDC | 51808-209 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Thyrotropin Releasing Hormone |
| Dosage Form Name | SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20120619 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | AnazaoHealth Corporation |
| Substance Name | PROTIRELIN |
| Strength Number | 500 |
| Strength Unit | ug/mL |
| Pharmaceutical Classes |