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Phentermine Hydrochloride
Phentermine Hydrochloride - 51224-101-50 - (Phentermine Hydrochloride)
Drug Information of Phentermine Hydrochloride
| Product NDC: | 51224-101 |
| Proprietary Name: | Phentermine Hydrochloride |
| Non Proprietary Name: | Phentermine Hydrochloride |
| Active Ingredient(s): | 37.5 mg/1 & nbsp; Phentermine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Phentermine Hydrochloride
| Product NDC: | 51224-101 |
| Labeler Name: | TAGI Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA200272 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110308 |
Package Information of Phentermine Hydrochloride
| Package NDC: | 51224-101-50 |
| Package Description: | 100 TABLET in 1 BOTTLE (51224-101-50) |
NDC Information of Phentermine Hydrochloride
| NDC Code | 51224-101-50 |
| Proprietary Name | Phentermine Hydrochloride |
| Package Description | 100 TABLET in 1 BOTTLE (51224-101-50) |
| Product NDC | 51224-101 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Phentermine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110308 |
| Marketing Category Name | ANDA |
| Labeler Name | TAGI Pharma, Inc. |
| Substance Name | PHENTERMINE HYDROCHLORIDE |
| Strength Number | 37.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC] |
