NDC 43063-851 – Oxybutynin Chloride
Oxybutynin Chloride 5 mg/1 · Tablet · Oral
Product NDC43063-851
Product details
- Brand name
- Oxybutynin Chloride
- Generic name
- Oxybutynin Chloride
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA209335
- Marketed since
- December 22, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Cholinergic Muscarinic Antagonist
Active ingredients
- Oxybutynin Chloride 5 mg/1
Uses, dosage, side effects and warnings for Oxybutynin Chloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 43063-851-01 | 100 TABLET in 1 BOTTLE, PLASTIC (43063-851-01) | Mar 21, 2019 |
| 43063-851-60 | 60 TABLET in 1 BOTTLE, PLASTIC (43063-851-60) | Jun 11, 2018 |
| 43063-851-90 | 90 TABLET in 1 BOTTLE, PLASTIC (43063-851-90) | Jun 11, 2018 |
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