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PHENTERMINE HYDROCHLORIDE
PHENTERMINE HYDROCHLORIDE - 55289-791-07 - (phentermine hydrochloride)
Drug Information of PHENTERMINE HYDROCHLORIDE
| Product NDC: | 55289-791 |
| Proprietary Name: | PHENTERMINE HYDROCHLORIDE |
| Non Proprietary Name: | phentermine hydrochloride |
| Active Ingredient(s): | 15 mg/1 & nbsp; phentermine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PHENTERMINE HYDROCHLORIDE
| Product NDC: | 55289-791 |
| Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040886 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19970428 |
Package Information of PHENTERMINE HYDROCHLORIDE
| Package NDC: | 55289-791-07 |
| Package Description: | 7 CAPSULE in 1 BOTTLE, PLASTIC (55289-791-07) |
NDC Information of PHENTERMINE HYDROCHLORIDE
| NDC Code | 55289-791-07 |
| Proprietary Name | PHENTERMINE HYDROCHLORIDE |
| Package Description | 7 CAPSULE in 1 BOTTLE, PLASTIC (55289-791-07) |
| Product NDC | 55289-791 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | phentermine hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19970428 |
| Marketing Category Name | ANDA |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Substance Name | PHENTERMINE HYDROCHLORIDE |
| Strength Number | 15 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC] |
