62175-272 : Oxybutynin Chloride 15 mg 24 Hr Extended Release Tablet

NDC:	62175-272
Labeler:	Kremers Urban Pharmaceuticals Inc.
Product Type:	Human Prescription Drug
Drug Name:	Oxybutynin Chloride Extended Release
Dosage Form:	Oral Tablet, Extended Release
Application #:	ANDA078503
Rev. Date:	Mar 1, 2009

Appearance:

Markings:	KU;272
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.

KU 272: (62175-272) Oxybutynin Chloride 15 mg 24 Hr Extended Release Tablet by Kremers Urban Pharmaceuticals Inc.

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:

62175-272-32: 30 TABLET, EXTENDED RELEASE IN 1 BOTTLE (62175‑272‑32)
62175-272-37: 100 TABLET, EXTENDED RELEASE IN 1 BOTTLE (62175‑272‑37)
62175-272-41: 500 TABLET, EXTENDED RELEASE IN 1 BOTTLE (62175‑272‑41)
62175-272-43: 1000 TABLET, EXTENDED RELEASE IN 1 BOTTLE (62175‑272‑43)

Active Ingredients:

Oxybutynin Chloride

Dosage Strength:

15 mg

Inactive Ingredients:

Anhydrous Lactose
Lactose Monohydrate
Mannitol
Anhydrous Dextrose
Tartaric Acid
Silicon Dioxide
Magnesium Stearate
Cellulose Acetate
Polyethylene Glycol 400
Titanium Dioxide
Ferrosoferric Oxide
Propylene Glycol
Hypromellose 2208 (100 Mpa.s)
Triacetin

Pharmaceutical Classes:

Cholinergic Muscarinic Antagonist [EPC]
Cholinergic Muscarinic Antagonists [MoA]

NDC QR Code

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NDC 62175-272 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.