oxybutynin is a Oral Tablet, Film Coated, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Cadila Healthcare Limited. The primary component is Oxybutynin Chloride.
Product ID | 70771-1086_0dc00bfe-5c56-444c-87c0-9511deec2414 |
NDC | 70771-1086 |
Product Type | Human Prescription Drug |
Proprietary Name | oxybutynin |
Generic Name | Oxybutynin |
Dosage Form | Tablet, Film Coated, Extended Release |
Route of Administration | ORAL |
Marketing Start Date | 2017-08-10 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA202332 |
Labeler Name | Cadila Healthcare Limited |
Substance Name | OXYBUTYNIN CHLORIDE |
Active Ingredient Strength | 5 mg/1 |
Pharm Classes | Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2017-08-10 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA202332 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2017-08-10 |
Marketing Category | ANDA |
Application Number | ANDA202332 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2017-08-10 |
Marketing Category | ANDA |
Application Number | ANDA202332 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2017-08-10 |
Marketing Category | ANDA |
Application Number | ANDA202332 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2017-08-10 |
Marketing Category | ANDA |
Application Number | ANDA202332 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2017-08-10 |
Marketing Category | ANDA |
Application Number | ANDA202332 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2017-08-10 |
Marketing Category | ANDA |
Application Number | ANDA202332 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2017-08-10 |
Ingredient | Strength |
---|---|
OXYBUTYNIN CHLORIDE | 5 mg/1 |
SPL SET ID: | f405a774-bd91-4513-b7c7-c44f0596d988 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
0615-8219 | oxybutynin | oxybutynin |
0615-8220 | Oxybutynin | Oxybutynin |
50090-5352 | oxybutynin | oxybutynin |
50090-5353 | oxybutynin | oxybutynin |
68382-255 | oxybutynin | oxybutynin |
68382-256 | oxybutynin | oxybutynin |
68382-257 | oxybutynin | oxybutynin |
70518-1457 | oxybutynin | oxybutynin |
70518-2331 | oxybutynin | oxybutynin |
70771-1086 | oxybutynin | oxybutynin |
70771-1087 | oxybutynin | oxybutynin |
70771-1088 | oxybutynin | oxybutynin |
71335-0974 | oxybutynin | oxybutynin |
0023-6153 | OXYTROL | Oxybutynin |
52544-920 | OXYTROL | Oxybutynin |
0023-9637 | Oxytrol for Women | Oxybutynin |
52544-166 | Oxytrol For Women | oxybutynin |