68788-6424 : Venlafaxine Hydrochloride 75 mg Oral Capsule, Extended Release
NDC: | 68788-6424 |
Labeler: | Preferred Pharmaceuticals Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Venlafaxine Hydrochloride |
Dosage Form: | Oral Capsule, Extended Release |
Application #: | ANDA090174 |
Rev. Date: |
Appearance:
Markings: | ZA;36;75;mg |
Shapes: |
Capsule |
Colors: |
Orange /
White |
Size (mm): | 20 |
Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. |
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.
NDC Package Codes:
- 68788-6424-1: 100 CAPSULE, EXTENDED RELEASE IN 1 BOTTLE (68788‑6424‑1)
- 68788-6424-2: 20 CAPSULE, EXTENDED RELEASE IN 1 BOTTLE (68788‑6424‑2)
- 68788-6424-3: 30 CAPSULE, EXTENDED RELEASE IN 1 BOTTLE (68788‑6424‑3)
- 68788-6424-6: 60 CAPSULE, EXTENDED RELEASE IN 1 BOTTLE (68788‑6424‑6)
- 68788-6424-8: 120 CAPSULE, EXTENDED RELEASE IN 1 BOTTLE (68788‑6424‑8)
- 68788-6424-9: 90 CAPSULE, EXTENDED RELEASE IN 1 BOTTLE (68788‑6424‑9)
Active Ingredients:
- Venlafaxine Hydrochloride
Dosage Strength:
- 75 mg
Inactive Ingredients:
- Silicon Dioxide
- Cetostearyl Alcohol
- Gelatin
- Hypromelloses
- Cellulose, Microcrystalline
- Ethyl Acrylate and Methyl Methacrylate Copolymer (2:1
- 750000 Mw)
- Sodium Lauryl Sulfate
- Talc
- Titanium Dioxide
- Ferric Oxide Red
- Ferrosoferric Oxide
Pharmaceutical Classes:
- Norepinephrine Uptake Inhibitors [MoA]
- Serotonin Uptake Inhibitors [MoA]
- Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Related Products:
Based on records with the same trade name.- 68788-6806 Venlafaxine Hydrochloride 150 mg Oral Capsule, Extended Release by Preferred Pharmaceuticals Inc.
- 68788-6834 Venlafaxine Hydrochloride 37.5 mg Oral Capsule, Extended Release by Preferred Pharmaceuticals Inc.
- 68788-7891 Venlafaxine Hydrochloride 37.5 mg Oral Capsule, Extended Release by Preferred Pharmaceuticals Inc.
- 68788-7919 Venlafaxine Hydrochloride 37.5 mg Oral Capsule, Extended Release by Preferred Pharmaceuticals Inc.
- 68788-8140 Venlafaxine Hydrochloride 75 mg Oral Capsule, Extended Release by Preferred Pharmaceuticals Inc.
- 68788-8682 Venlafaxine Hydrochloride 37.5 mg Oral Capsule, Extended Release by Preferred Pharmaceuticals Inc.
- 68788-8694 Venlafaxine Hydrochloride 75 mg Oral Capsule, Extended Release by Preferred Pharmaceuticals Inc.
- 68788-8917 Venlafaxine Hydrochloride 75 mg Oral Capsule, Extended Release by Preferred Pharmaceuticals Inc.
- 68788-8068 Venlafaxine Hydrochloride 75 mg Oral Capsule, Extended Release by Preferred Pharmaceuticals, Inc.
- 68788-8072 Venlafaxine Hydrochloride 150 mg Oral Capsule, Extended Release by Preferred Pharmaceuticals, Inc.
- 68788-9425 Venlafaxine Hydrochloride 37.5 mg Oral Capsule, Extended Release by Preferred Pharmaceuticals, Inc.
- 0093-0199 Venlafaxine 25 mg (As Venlafaxine Hydrochloride 28.3 mg) Oral Tablet by Teva Pharmaceuticals USA Inc
- 0093-7380 Venlafaxine 37.5 mg (As Venlafaxine Hydrochloride 42.5 mg) Oral Tablet by Teva Pharmaceuticals USA Inc
- 0093-7381 Venlafaxine 50 mg (As Venlafaxine Hydrochloride 56.6 mg) Oral Tablet by Teva Pharmaceuticals USA Inc
- 0093-7382 Venlafaxine 75 mg (As Venlafaxine Hydrochloride 84.9 mg) Oral Tablet by Teva Pharmaceuticals USA Inc
- 0093-7383 Venlafaxine 100 mg (As Venlafaxine Hydrochloride 113 mg) Oral Tablet by Teva Pharmaceuticals USA Inc
- 0093-7384 Venlafaxine (As Venlafaxine Hydrochloride) 37.5 mg 24 Hr Extended Release Capsule by Teva Pharmaceuticals USA Inc
- 0093-7385 Venlafaxine (As Venlafaxine Hydrochloride) 75 mg 24 Hr Extended Release Capsule by Teva Pharmaceuticals USA Inc
- 0093-7386 Venlafaxine (As Venlafaxine Hydrochloride) 150 mg 24 Hr Extended Release Capsule by Teva Pharmaceuticals USA Inc
- 0093-9147 Venlafaxine Hydrochloride 25 mg Oral Tablet by Teva Pharmaceuticals USA, Inc.
- More related products ...
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.