Oxybutynin Chloride
- Product NDC
- 68151-9200
- 11-digit product format
- 681519200
- Labeler code
- 68151
- Product ID
- 68151-9200_a67cb47d-630d-4d9e-9b5f-8526b9256593
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxybutynin Chloride
- Dosage form
- SYRUP
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA074868
- Marketing category
- ANDA
- Marketing start
- 1997-02-12
- Marketing end
- 0000-00-00
- Substance
- OXYBUTYNIN CHLORIDE
- Active strength
- 5 mg/5mL
- Pharmacologic classes
- Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68151-9200-1 | Oxybutynin Chloride | 5 mL in 1 SYRINGE, PLASTIC | SYRUP | 5 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-9200 | OXYBUTYNIN CHLORIDE SYRUP [CARILION MATERIALS MANAGEMENT] | 4 | Legacy NDC, 1 package rows | 20181231_43cb979d-b532-43cf-9cd9-de66ebb6a539.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 68151-9200-1 | 68151920001 | 5 mL in 1 SYRINGE, PLASTIC | 5 ml | Historical |