51407-192 : Ezetimibe and Simvastatin Oral Tablet
| NDC: | 51407-192 |
| Labeler: | Golden State Medical Supply Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: | Ezetimibe and Simvastatin |
| Dosage Form: | Oral Tablet |
| Application #: | ANDA200909 |
| Rev. Date: |
Appearance:
| Markings: | T101 |
| Shapes: |
Round |
| Colors: |
White |
| Size (mm): | 7 |
| 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. | |
NDC Package Codes:
- 51407-206-05: 500 TABLET, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (51407‑206‑05)
- 51407-206-30: 30 TABLET, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (51407‑206‑30)
- 51407-206-90: 90 TABLET, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (51407‑206‑90)
Active Ingredients:
- Bupropion Hydrochloride
Dosage Strength:
- 150 mg
Inactive Ingredients:
- Hypromellose 2910 (15 Mpa.s)
- Glyceryl Dibehenate
- Hydroxypropyl Cellulose, Unspecified
- Silicon Dioxide
- Ethylcellulose (100 Mpa.s)
- Povidone, Unspecified
- Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
- Triethyl Citrate
- Ferrosoferric Oxide
- Propylene Glycol /
Pharmaceutical Classes:
- Aminoketone [EPC]
- Dopamine Uptake Inhibitors [MoA]
- Increased Dopamine Activity [PE]
- Increased Norepinephrine Activity [PE]
- Norepinephrine Uptake Inhibitors [MoA]
Related Products:
Based on records with the same trade name.- 51407-207 Bupropion Hydrochloride (Xl) 300 mg Oral Tablet, Extended Release by Golden State Medical Supply Inc.
- 0527-2415 Bupropion Hydrochloride (Xl) (Xl) 150 mg Oral Tablet, Extended Release by Lannett Company Inc.
- 0527-2430 Bupropion Hydrochloride (Xl) (Xl) 300 mg Oral Tablet, Extended Release by Lannett Company Inc.
- 0615-8179 Bupropion Hydrochloride (Xl) 300 mg Oral Tablet, Extended Release by Ncs Healthcare of Ky, Inc Dba Vangard Labs
- 0615-8241 Bupropion Hydrochloride (Xl) 150 mg Oral Tablet, Extended Release by Ncs Healthcare of Ky, Inc Dba Vangard Labs
- 0615-8416 Bupropion Hydrochloride XL 150 mg Oral Tablet, Extended Release by Ncs Healthcare of Ky, LLC Dba Vangard Labs
- 0615-8418 Bupropion Hydrochloride XL 300 mg Oral Tablet, Extended Release by Ncs Healthcare of Ky, LLC Dba Vangard Labs
- 0781-5528 Bupropion Hydrochloride (Xl) (Xl) 150 mg Oral Tablet, Extended Release by Sandoz Inc.
- 0781-5529 Bupropion Hydrochloride (Xl) (Xl) 300 mg Oral Tablet, Extended Release by Sandoz Inc.
- 0904-7084 Bupropion Hydrochloride XL 150 mg Oral Tablet, Extended Release by Major Pharmaceuticals
- 24979-101 Bupropion Hydrochloride (Xl) 150 mg Oral Tablet, Extended Release by Twi Pharmaceuticals, Inc.
- 24979-102 Bupropion Hydrochloride (Xl) 300 mg Oral Tablet, Extended Release by Twi Pharmaceuticals, Inc.
- 42806-348 Bupropion Hydrochloride XL 150 mg Oral Tablet, Extended Release by Epic Pharma, LLC
- 42806-349 Bupropion Hydrochloride XL 300 mg Oral Tablet, Extended Release by Epic Pharma, LLC
- 42806-414 Bupropion Hydrochloride XL 150 mg Oral Tablet, Extended Release by Epic Pharma, LLC
- 42806-416 Bupropion Hydrochloride XL 300 mg Oral Tablet, Extended Release by Epic Pharma, LLC
- 43598-655 Bupropion Hydrochloride (Xl) 150 mg Oral Tablet, Film Coated, Extended Release by Dr Reddys Laboratories Inc
- 43598-656 Bupropion Hydrochloride (Xl) 300 mg Oral Tablet, Film Coated, Extended Release by Dr Reddys Laboratories Inc
- 43826-067 Bupropion Hydrochloride (Xl) 150 mg Oral Tablet, Extended Release by Bora Pharmaceutical Laboratories Inc.
- 43826-068 Bupropion Hydrochloride (Xl) 300 mg Oral Tablet, Extended Release by Bora Pharmaceutical Laboratories 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.
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