10370-101 : Bupropion Hydrochloride XL 150 mg 24 Hr Extended Release Tablet
NDC: | 10370-101 |
Labeler: | Par Pharmaceutical, Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | ![]() |
Dosage Form: | Oral Tablet, Film Coated, Extended Release |
Application #: | ANDA077284 |
Rev. Date: |
Appearance:
Markings: | A101 |
Shapes: |
Round |
Colors: |
![]() |
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. |
![A101: (10370-101) Bupropion Hydrochloride XL 150 mg 24 Hr Extended Release Tablet by Par Pharmaceutical, Inc. A101: (10370-101) Bupropion Hydrochloride XL 150 mg 24 Hr Extended Release Tablet by Par Pharmaceutical, Inc.](/images/NDC/10370-101.jpg)
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:
- 10370-101-00: 1000 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (10370‑101‑00)
- 10370-101-03: 30 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (10370‑101‑03)
- 10370-101-06: 60 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (10370‑101‑06)
- 10370-101-09: 90 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (10370‑101‑09)
- 10370-101-50: 500 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (10370‑101‑50)
Active Ingredients:
- Bupropion Hydrochloride
Dosage Strength:
- 150 mg
Inactive Ingredients:
- Alcohol
- Ethylcelluloses
- Hydroxypropyl Cellulose
- Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
- Povidone
- Silicon Dioxide
- Hydrochloric Acid
- Isopropyl Alcohol
- Hydrogenated Cottonseed Oil
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.- 10370-102 Bupropion Hydrochloride XL 300 mg 24 Hr Extended Release Tablet by Par Pharmaceutical, Inc.
- 10370-159 Bupropion Hydrochloride 100 mg 12 Hr Extended Release Tablet by Par Pharmaceuticals, Inc.
- 10370-160 Bupropion Hydrochloride 150 mg 12 Hr Extended Release Tablet by Par Pharmaceuticals, Inc.
- 10370-161 Bupropion Hydrochloride 200 mg 12 Hr Extended Release Tablet by Par Pharmaceuticals, Inc.
- 10370-204 Bupropion Hydrochloride 150 mg 12 Hr Extended Release Tablet by Anchen Pharmaceuticals, Inc.
- 0115-5445 Bupropion Hydrochloride 200 mg 12 Hr Extended Release Tablet by Global Pharmaceuticals, Division of Impax Laboratories Inc.
- 0115-6811 Bupropion Hydrochloride XL 150 mg 24 Hr Extended Release Tablet by Global Pharmaceuticals, Division of Impax Laboratories, Inc.
- 0179-0022 Bupropion Hydrochloride 100 mg 12 Hr Extended Release Tablet by Kaiser Foundation Hospitals
- 0179-0025 Bupropion Hydrochloride 75 mg Oral Tablet by Kaiser Foundation Hospitals
- 0179-0030 Bupropion Hydrochloride 150 mg 12 Hr Extended Release Tablet by Kaiser Foundation Hospitals
- 0185-0410 Bupropion Hydrochloride 100 mg 12 Hr Extended Release Tablet by Eon Labs, Inc.
- 0185-0415 Bupropion Hydrochloride 150 mg 12 Hr Extended Release Tablet by Eon Labs, Inc.
- 0185-1111 Bupropion Hydrochloride 200 mg 12 Hr Extended Release Tablet by Eon Labs, Inc.
- 0378-0433 Bupropion Hydrochloride 75 mg Oral Tablet by Mylan Pharmaceuticals Inc.
- 0378-0435 Bupropion Hydrochloride 100 mg Oral Tablet by Mylan Pharmaceuticals Inc.
- 0378-2008 Bupropion Hydrochloride XL 150 mg 24 Hr Extended Release Tablet by Mylan Pharmaceuticals Inc.
- 0378-2009 Bupropion Hydrochloride XL 300 mg 24 Hr Extended Release Tablet by Mylan Pharmaceuticals Inc.
- 0378-3411 Bupropion Hydrochloride 100 mg 12 Hr Extended Release Tablet by Mylan Pharmaceuticals Inc.
- 0378-3412 Bupropion Hydrochloride 150 mg 12 Hr Extended Release Tablet by Mylan Pharmaceuticals Inc.
- 0378-3413 Bupropion Hydrochloride 200 mg 12 Hr Extended Release Tablet by Mylan Pharmaceuticals Inc.
- More related products ...
NDC QR Code
Scan the QR code below to easily reference this data in the future:![NDC 10370-101 QR Code](/images/NDC-QR/10370-101-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.