Product NDC: | 21695-509 |
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) |
Product NDC: | 21695-509 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040886 |
Marketing Category: | ANDA |
Start Marketing Date: | 19991108 |
Package NDC: | 21695-509-00 |
Package Description: | 100 CAPSULE in 1 BOTTLE (21695-509-00) |
NDC Code | 21695-509-00 |
Proprietary Name | PHENTERMINE HYDROCHLORIDE |
Package Description | 100 CAPSULE in 1 BOTTLE (21695-509-00) |
Product NDC | 21695-509 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | PHENTERMINE HYDROCHLORIDE |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 19991108 |
Marketing Category Name | ANDA |
Labeler Name | Rebel Distributors Corp |
Substance Name | PHENTERMINE HYDROCHLORIDE |
Strength Number | 15 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC] |