Temozolomide 47335-0890
Product NDC
47335-0890- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 13, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA201742
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Temozolomide | 5 mg/1 |
Drug Class
Alkylating Drug [EPC]Alkylating Activity [MoA]Alkylating Drug [EPC]
Packaging Options(6)
1 BOTTLE in 1 CARTON (47335-890-21) / 14 CAPSULE in 1 BOTTLE
15 BLISTER PACK in 1 CARTON (47335-890-72) / 1 CAPSULE in 1 BLISTER PACK
5 BLISTER PACK in 1 CARTON (47335-890-74) / 1 CAPSULE in 1 BLISTER PACK
20 BLISTER PACK in 1 CARTON (47335-890-75) / 1 CAPSULE in 1 BLISTER PACK
1 BOTTLE in 1 CARTON (47335-890-80) / 5 CAPSULE in 1 BOTTLE
1 BOTTLE in 1 CARTON (47335-890-87) / 20 CAPSULE in 1 BOTTLE