68788-7109 : Oxybutynin Chloride 15 mg Oral Tablet, Extended Release

NDC:	68788-7109
Labeler:	Preferred Pharmaceuticals Inc.
Product Type:	Human Prescription Drug
Drug Name:	Oxybutynin Chloride
Dosage Form:	Oral Tablet, Extended Release
Application #:	ANDA207138
Rev. Date:	Mar 8, 2018

Appearance:

Markings:	EM3
Shapes:	Round
Colors:	Gray
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.

NDC Package Codes:

68788-7109-1: 100 TABLET, EXTENDED RELEASE IN 1 BOTTLE (68788‑7109‑1)
68788-7109-2: 20 TABLET, EXTENDED RELEASE IN 1 BOTTLE (68788‑7109‑2)
68788-7109-3: 30 TABLET, EXTENDED RELEASE IN 1 BOTTLE (68788‑7109‑3)
68788-7109-6: 60 TABLET, EXTENDED RELEASE IN 1 BOTTLE (68788‑7109‑6)
68788-7109-9: 90 TABLET, EXTENDED RELEASE IN 1 BOTTLE (68788‑7109‑9)

Active Ingredients:

Oxybutynin Chloride

Dosage Strength:

15 mg

Inactive Ingredients:

Silicon Dioxide
Hypromellose, Unspecified
Magnesium Stearate
Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
Microcrystalline Cellulose
Polyethylene Glycol, Unspecified
Sodium Bicarbonate
Sodium Lauryl Sulfate
Talc
Titanium Dioxide
Triethyl Citrate
Ferric Oxide Yellow
Ferrosoferric Oxide /

Pharmaceutical Classes:

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

NDC QR Code

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NDC 68788-7109 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.