10702-014 : Betaxolol Hydrochloride (Betaxolol 17.88 mg) Oral Tablet
| NDC: | 10702-014 |
| Labeler: | Kvk-tech, Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Betaxolol Hydrochloride |
| Dosage Form: | Oral Tablet, Coated |
| Application #: | ANDA078962 |
| Rev. Date: |
Appearance:
| Markings: | K;14 |
| Shapes: |
Round |
| Colors: |
 White |
| Size (mm): | 9 |
| 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:
- 10702-014-01: 100 TABLET, COATED IN 1 BOTTLE (10702‑014‑01)
Active Ingredients:
- Betaxolol Hydrochloride
Dosage Strength:
- 20 mg
Inactive Ingredients:
- Lactose
- Cellulose, Microcrystalline
- Starch, Corn
- Sodium Starch Glycolate Type a Potato
- Stearic Acid
- Titanium Dioxide
- Polyethylene Glycol 400
- Polysorbate 80
- Carnauba Wax
- Hypromellose 2910 (6 Mpa.s)
Pharmaceutical Classes:
- Adrenergic beta-Antagonists [MoA]
- beta-Adrenergic Blocker [EPC]
Related Products:
Based on records with the same trade name.- 10702-013 Betaxolol Hydrochloride 10 mg (Betaxolol 8.94 mg) Oral Tablet by Kvk-tech, Inc.
- 61314-245 Betaxolol Hydrochloride 5.6 mg/ml Ophthalmic Solution/ Drops by Falcon Pharmaceuticals, Ltd.
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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.