oxybutynin chloride
- Product NDC
- 50090-4307
- 11-digit product format
- 500904307
- Labeler code
- 50090
- Product ID
- 50090-4307_9e1b91d5-d9c0-4b55-b5d5-048879327725
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oxybutynin chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA207138
- Marketing category
- ANDA
- Marketing start
- 2016-12-20
- Substance
- OXYBUTYNIN CHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- oxybutynin chloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OXYBUTYNIN CHLORIDE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L9F3D9RENQ |
| Rxcui | 863619 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-4307-0 | oxybutynin chloride | 90 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 90 | | 10 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4307 | OXYBUTYNIN CHLORIDE TABLET, EXTENDED RELEASE [A-S MEDICATION SOLUTIONS] | 10 | Current NDC, Legacy NDC, 1 package rows | 20240604_8f147f73-cfc6-40a3-b1a3-e4cab1868523.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4307-0 | 50090430700 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-4307-0) | 2019-05-23 | 0000-00-00 | No | No | Current |