Cyclophosphamide
- Product NDC
- 68001-370
- 11-digit product format
- 680010370
- Labeler code
- 68001
- Product ID
- 68001-370_c688325c-7953-590a-e053-2995a90a50e0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyclophosphamide
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAVENOUS; ORAL
- Labeler
- BluePoint Laboratories
- Application
- ANDA210046
- Marketing category
- ANDA
- Marketing start
- 2018-05-31
- Marketing end
- 2022-03-31
- Substance
- CYCLOPHOSPHAMIDE
- Active strength
- 500 mg/25mL
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68001-370-27 | 68001037027 | 1 VIAL, SINGLE-DOSE in 1 CARTON (68001-370-27) > 25 mL in 1 VIAL, SINGLE-DOSE (68001-370-24) | 2018-11-23 | 0000-00-00 | No | No | Current |