Theophylline 70095-0017
Product NDC
70095-0017- Manufacturer
- Sun Pharmaceutical Industries Limited
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 22, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA214806
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Theophylline Anhydrous | 300 mg/1 |
Drug Class
Methylxanthine [EPC]Methylxanthine [EPC]Xanthines [CS]
Packaging Options(1)
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70095-017-01)