Oxybutynin Chloride
- Product NDC
- 17856-1491
- 11-digit product format
- 178561491
- Labeler code
- 17856
- Product ID
- 17856-1491_4313b89a-66f8-4d1c-abfe-4e52a7bd1a0b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oxybutynin chloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Atlantic Biologicals Corps
- Application
- ANDA076682
- Marketing category
- ANDA
- Marketing start
- 2004-12-28
- 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
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 17856-1491-5 | Oxybutynin Chloride | 5 mL in 1 CUP | SOLUTION | 5 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17856-1491 | OXYBUTYNIN CHLORIDE SOLUTION [ATLANTIC BIOLOGICALS CORPS] | 2 | Legacy NDC, 1 package rows | 20160504_e710a298-4c71-43a1-a152-76550d596667.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 17856-1491-5 | 17856149105 | 5 mL in 1 CUP | 5 ml | Historical |