NDC 70771-1087 – Oxybutynin
Oxybutynin Chloride 10 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC70771-1087
Product details
- Brand name
- Oxybutynin
- Generic name
- Oxybutynin
- Labeler
- Zydus Lifesciences Limited
- 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 (6)
| Package NDC | Description | Since |
|---|---|---|
| 70771-1087-1 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1087-1) | Aug 10, 2017 |
| 70771-1087-3 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1087-3) | Aug 10, 2017 |
| 70771-1087-4 | 10 BLISTER PACK in 1 CARTON (70771-1087-4) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70771-1087-2) | Aug 10, 2017 |
| 70771-1087-5 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1087-5) | Aug 10, 2017 |
| 70771-1087-6 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1087-6) | Aug 10, 2017 |
| 70771-1087-9 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1087-9) | Aug 10, 2017 |
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- 68382-255 Oxybutynin Chloride 5 mg/1 · Tablet, Film Coated, Extended Release · Zydus Pharmaceuticals USA Inc.
- 68382-256 Oxybutynin Chloride 10 mg/1 · Tablet, Film Coated, Extended Release · Zydus Pharmaceuticals USA Inc.
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