69097-877 : Bupropion Hydrochloride 100 mg Oral Tablet, Extended Release
NDC: | 69097-877 |
Labeler: | Cipla USA Inc., |
Product Type: | Human Prescription Drug |
Dosage Form: | Oral Tablet, Extended Release |
Application #: | ANDA206674 |
Rev. Date: |
Appearance:
Markings: | IG;484 |
Shapes: |
Round |
Colors: |
![]() |
Size (mm): | 10 |
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:
- 69097-877-02: 30 TABLET, EXTENDED RELEASE IN 1 BOTTLE (69097‑877‑02)
- 69097-877-03: 60 TABLET, EXTENDED RELEASE IN 1 BOTTLE (69097‑877‑03)
- 69097-877-07: 100 TABLET, EXTENDED RELEASE IN 1 BOTTLE (69097‑877‑07)
- 69097-877-12: 500 TABLET, EXTENDED RELEASE IN 1 BOTTLE (69097‑877‑12)
Active Ingredients:
- Bupropion Hydrochloride
Dosage Strength:
- 100 mg
Inactive Ingredients:
- Cellulose, Microcrystalline
- Silicon Dioxide
- Hypromelloses
- Hydrochloric Acid
- Magnesium Stearate
- Titanium Dioxide
- Polyethylene Glycol, Unspecified
- Polysorbate 80
- Fd&c Blue No. 1
Pharmaceutical Classes:
- Aminoketone [EPC]
- Dopamine Uptake Inhibitors [MoA]
- Increased Dopamine Activity [PE]
- Increased Norepinephrine Activity [PE]
- Norepinephrine Uptake Inhibitors [MoA]
NDC QR Code
Scan the QR code below to easily reference this data in the future:![NDC 69097-877 QR Code](/images/NDC-QR/69097-877-QR.png)
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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.