Oxybutynin Chloride
- Product NDC
- 67296-1175
- 11-digit product format
- 672961175
- Labeler code
- 67296
- Product ID
- 67296-1175_d60ff571-d1c7-0675-e053-2995a90a15aa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxybutynin Chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA074625
- Marketing category
- ANDA
- Marketing start
- 2011-11-07
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- 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 |
|---|
| 67296-1175-3 | Oxybutynin Chloride | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1175 | OXYBUTYNIN CHLORIDE TABLET [REDPHARM DRUG, INC.] | 3 | Legacy NDC, 1 package rows | 20220121_4eb9441b-27ba-1b8f-e054-00144ff88e88.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 |
|---|
| 67296-1175-3 | 67296117503 | 30 TABLET in 1 BOTTLE (67296-1175-3) | 30 tablet | 2011-11-07 | 0000-00-00 | No | No | Current |