NDC 10702-201 – Oxybutynin Chloride
Oxybutynin Chloride 5 mg/1 · Tablet · Oral
Product NDC10702-201
Product details
- Brand name
- Oxybutynin Chloride
- Generic name
- Oxybutynin Chloride
- Labeler
- KVK-Tech, 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 |
|---|---|---|
| 10702-201-01 | 100 TABLET in 1 BOTTLE, PLASTIC (10702-201-01) | Dec 22, 2017 |
| 10702-201-10 | 1000 TABLET in 1 BOTTLE, PLASTIC (10702-201-10) | Dec 22, 2017 |
| 10702-201-50 | 500 TABLET in 1 BOTTLE, PLASTIC (10702-201-50) | Dec 22, 2017 |
Recalls mentioning this NDC
- D-0340-2019 Dec 26, 2018 · Class II
Labeling: Wrong bar code
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