Oxybutynin Chloride
- Product NDC
- 70934-909
- 11-digit product format
- 709340909
- Labeler code
- 70934
- Product ID
- 70934-909_d5e2a838-edcc-1d42-e053-2995a90a9703
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxybutynin Chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA209823
- Marketing category
- ANDA
- Marketing start
- 2021-10-06
- 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
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 70934-909-30 | 70934090930 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-909-30) | 30 tablet | 2022-01-18 | 0000-00-00 | No | No | Current |
| 70934-909-60 | 70934090960 | 60 TABLET in 1 BOTTLE, PLASTIC (70934-909-60) | 60 tablet | 2021-10-06 | 0000-00-00 | No | No | Current |