NDC 70954-005 – Oxybutynin Chloride
Oxybutynin Chloride 5 mg/1 · Tablet · Oral
Product NDC70954-005
Product details
- Brand name
- Oxybutynin Chloride
- Generic name
- Oxybutynin Chloride
- Labeler
- ANI Pharmaceuticals, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA209823
- Marketed since
- November 15, 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 70954-005-10 | 100 TABLET in 1 BOTTLE (70954-005-10) | Nov 15, 2017 |
| 70954-005-20 | 500 TABLET in 1 BOTTLE (70954-005-20) | Nov 15, 2017 |
| 70954-005-30 | 1000 TABLET in 1 BOTTLE (70954-005-30) | Nov 15, 2017 |
| 70954-005-50 | 100 BLISTER PACK in 1 CARTON (70954-005-50) / 1 TABLET in 1 BLISTER PACK (70954-005-40) | Aug 20, 2021 |
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