Acetazolamide 51672-4023
Product NDC
51672-4023- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 28, 1997
- Listing Expires
- December 31, 2026
- Application
- ANDA040195
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Acetazolamide | 250 mg/1 |
Drug Class
Carbonic Anhydrase Inhibitor [EPC]Carbonic Anhydrase Inhibitor [EPC]Carbonic Anhydrase Inhibitors [MoA]
Packaging Options(1)
100 TABLET in 1 BOTTLE (51672-4023-1)