43353-769 : Oxybutynin Chloride 10 mg 24 Hr Extended Release Tablet
NDC: | 43353-769 |
Labeler: | Aphena Pharma Solutions - Tennessee, Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Oxybutynin Chloride |
Dosage Form: | Oral Tablet, Film Coated, Extended Release |
Application #: | ANDA078503 |
Rev. Date: |
Appearance:
Markings: | 271;KU |
Shapes: |
Round |
Colors: |
White |
Size (mm): | 8 |
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:
- 43353-769-41: 1600 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (43353‑769‑41)
Active Ingredients:
- Oxybutynin Chloride
Dosage Strength:
- 10 mg
Inactive Ingredients:
- Anhydrous Lactose
- Lactose Monohydrate
- Mannitol
- Anhydrous Dextrose
- Tartaric Acid
- Silicon Dioxide
- Magnesium Stearate
- Cellulose Acetate
- Polyethylene Glycol
- Titanium Dioxide
- Triacetin
- Ferrosoferric Oxide
- Propylene Glycol
- Hypromelloses
Pharmaceutical Classes:
- Cholinergic Muscarinic Antagonist [EPC]
- Cholinergic Muscarinic Antagonists [MoA]
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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.