OXYBUTYNIN CHLORIDE
- Product NDC
- 72189-130
- 11-digit product format
- 721890130
- Labeler code
- 72189
- Product ID
- 72189-130_2bece08b-b60b-a15e-e063-6394a90a3a13
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- OXYBUTYNIN CHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- direct rx
- Application
- ANDA071655
- Marketing category
- ANDA
- Marketing start
- 2020-11-11
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| L9F3D9RENQ | OXYBUTYNIN CHLORIDE | 1508-65-2 | OXYBUTYNIN CHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-130-30 | 72189013030 | 30 TABLET in 1 BOTTLE (72189-130-30) | 30 tablet | 2020-11-11 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| OXYBUTYNIN CHLORIDE | direct rx | 2025-01-17 | HUMAN PRESCRIPTION DRUG LABEL | 3 |