Oxybutynin Chloride
- Product NDC
- 68788-8141
- 11-digit product format
- 687888141
- Labeler code
- 68788
- Product ID
- 68788-8141_c96411f4-50fe-42a7-9463-5bb9d2939ac3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxybutynin Chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA209335
- Marketing category
- ANDA
- Marketing start
- 2022-02-11
- Substance
- OXYBUTYNIN CHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Oxybutynin Chloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OXYBUTYNIN CHLORIDE | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L9F3D9RENQ |
| Rxcui | 863664 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68788-8141-9 | Oxybutynin Chloride | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68788-8141 | OXYBUTYNIN CHLORIDE TABLET [PREFERRED PHARMACEUTICALS INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20240727_0e002fe8-fa3f-4a7d-84df-0c6e031e6ae4.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-8141-9 | 68788814109 | 90 TABLET in 1 BOTTLE, PLASTIC (68788-8141-9) | 90 tablet | 2022-02-11 | 0000-00-00 | No | No | Current |