43063-772 : Contrave Oral Tablet, Extended Release
NDC: | 43063-772 |
Labeler: | Pd-rx Pharmaceuticals, Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Contrave Extended-release |
Dosage Form: | Oral Tablet, Extended Release |
Application #: | NDA200063 |
Rev. Date: |
Appearance:
Markings: | NB;890 |
Shapes: |
Round |
Colors: |
Blue |
Size (mm): | 12 |
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:
- 43063-772-70: 70 TABLET, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (43063‑772‑70)
Active Ingredients:
- Naltrexone Hydrochloride
- Bupropion Hydrochloride
Dosage Strength:
- 8 mg
- 90 mg
Pharmaceutical Classes:
- Opioid Antagonist [EPC]
- Opioid Antagonists [MoA]
- 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.- 50090-2945 Contrave Oral Tablet, Extended Release by A-s Medication Solutions
- 51267-890 Contrave Oral Tablet, Extended Release by Orexigen Therapeutics, Inc.
NDC QR Code
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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.