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NDC 00023-5861-11 GELNIQUE 100 mg/g Details
GELNIQUE 100 mg/g
GELNIQUE is a TRANSDERMAL GEL in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Allergan, Inc.. The primary component is OXYBUTYNIN CHLORIDE.
MedlinePlus Drug Summary
Oxybutynin topical gel is used to treat overactive bladder (a condition in which the bladder muscles contract uncontrollably and cause frequent urination, urgent need to urinate, and inability to control urination)control frequent urination, urgent need to urinate, and urge urinary incontinence (sudden strong need to urinate that may cause urine leakage) in people who have overactive bladder OAB; condition in which the bladder muscles tighten uncontrollably to empty the bladder even when it is not full). Oxybutynin gel is in a class of medications called antimuscarinics. It works by relaxing the bladder muscles.
Related Packages: 00023-5861-11Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Oxybutynin Topical
Product Information
| NDC | 00023-5861 |
|---|---|
| Product ID | 0023-5861_ffa5a0e3-0166-49da-bfca-09199c0cae3e |
| Associated GPIs | 54100045204030 |
| GCN Sequence Number | 065081 |
| GCN Sequence Number Description | oxybutynin chloride GEL PACKET 10 % TRANSDERM |
| HIC3 | R1A |
| HIC3 Description | URINARY TRACT ANTISPASMODIC/ANTIINCONTINENCE AGENT |
| GCN | 21853 |
| HICL Sequence Number | 002048 |
| HICL Sequence Number Description | OXYBUTYNIN CHLORIDE |
| Brand/Generic | Brand |
| Proprietary Name | GELNIQUE |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | oxybutynin chloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | GEL |
| Route | TRANSDERMAL |
| Active Ingredient Strength | 100 |
| Active Ingredient Units | mg/g |
| Substance Name | OXYBUTYNIN CHLORIDE |
| Labeler Name | Allergan, Inc. |
| Pharmaceutical Class | Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA] |
| DEA Schedule | n/a |
| Marketing Category | NDA |
| Application Number | NDA022204 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 00023-5861-11 (00023586111)
| NDC Package Code | 0023-5861-11 |
|---|---|
| Billing NDC | 00023586111 |
| Package | 30 PACKET in 1 CARTON (0023-5861-11) / 1 g in 1 PACKET (0023-5861-10) |
| Marketing Start Date | 2017-04-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |