Temozolomide
- Product NDC
- 23155-777
- 11-digit product format
- 231550777
- Labeler code
- 23155
- Product ID
- 23155-777_e1982c81-2588-45cf-94f7-160a700709e0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Temozolomide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Application
- ANDA078879
- Marketing category
- ANDA
- Marketing start
- 2022-06-15
- Marketing end
- 0000-00-00
- Substance
- TEMOZOLOMIDE
- Active strength
- 140 mg/1
- Pharmacologic classes
- Alkylating Activity [MoA], Alkylating Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 23155-777-71 | 23155077771 | 5 CAPSULE in 1 BOTTLE (23155-777-71) | 5 capsule | 2022-06-15 | 0000-00-00 | No | No | Current |
| 23155-777-72 | 23155077772 | 14 CAPSULE in 1 BOTTLE (23155-777-72) | 14 capsule | 2022-06-15 | 0000-00-00 | No | No | Current |