Search by Drug Name or NDC
NDC 68788-7236-07 Phendimetrazine Tartrate 35 mg/1 Details
Phendimetrazine Tartrate 35 mg/1
Phendimetrazine Tartrate is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is PHENDIMETRAZINE TARTRATE.
Product Information
| NDC | 68788-7236 |
|---|---|
| Product ID | 68788-7236_d2d294ac-e7ec-4e00-a1c5-f43943a5165a |
| Associated GPIs | 61200050100305 |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Phendimetrazine Tartrate |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Phendimetrazine Tartrate |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 35 |
| Active Ingredient Units | mg/1 |
| Substance Name | PHENDIMETRAZINE TARTRATE |
| Labeler Name | Preferred Pharmaceuticals Inc. |
| Pharmaceutical Class | Appetite Suppression [PE], Increased Sympathetic Activity [PE], Sympathomimetic Amine Anorectic [EPC] |
| DEA Schedule | CIII |
| Marketing Category | ANDA |
| Application Number | ANDA091042 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 68788-7236-07 (68788723607)
| NDC Package Code | 68788-7236-7 |
|---|---|
| Billing NDC | 68788723607 |
| Package | 7 TABLET in 1 BOTTLE (68788-7236-7) |
| Marketing Start Date | 2018-08-13 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |