CYCLOPHOSPHAMIDE
- Product NDC
- 62559-931
- 11-digit product format
- 625590931
- Labeler code
- 62559
- Product ID
- 62559-931_cceec7d5-005a-4f04-9e40-d81e8123b944
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CYCLOPHOSPHAMIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- ANI Pharmaceuticals, Inc.
- Application
- ANDA207014
- Marketing category
- ANDA
- Marketing start
- 2020-06-22
- Marketing end
- 2023-08-31
- Substance
- CYCLOPHOSPHAMIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Alkylating Activity [MoA], Alkylating Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 62559-931-01 | 62559093101 | 100 CAPSULE in 1 BOTTLE (62559-931-01) | 100 capsule | 2020-06-22 | 0000-00-00 | No | No | Current |