NDC 0615-8220 – Oxybutynin
Oxybutynin Chloride 10 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC0615-8220
Product details
- Brand name
- Oxybutynin
- Generic name
- Oxybutynin
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA202332
- Marketed since
- August 10, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Cholinergic Muscarinic Antagonist
Active ingredients
- Oxybutynin Chloride 10 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0615-8220-39 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-8220-39) | Jun 28, 2018 |
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