OXYBUTYNIN CHLORIDE
- Product NDC
- 72189-132
- 11-digit product format
- 721890132
- Labeler code
- 72189
- Product ID
- 72189-132_2bece08b-b60c-a15e-e063-6394a90a3a13
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- OXYBUTYNIN CHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA207138
- Marketing category
- ANDA
- Marketing start
- 2020-08-24
- 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 |
|---|
| 72189-132-30 | OXYBUTYNIN CHLORIDE | 30 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-132 | OXYBUTYNIN CHLORIDE TABLET, EXTENDED RELEASE [DIRECT RX] | 2 | Current NDC, Legacy NDC, 1 package rows | 20250119_ada3be87-2cdd-75f7-e053-2995a90aa95b.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 |
|---|
| 72189-132-30 | 72189013230 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-132-30) | 2020-08-24 | 0000-00-00 | No | No | Current |