CYCLOPHOSPHAMIDE
- Product NDC
- 43975-308
- 11-digit product format
- 439750308
- Labeler code
- 43975
- Product ID
- 43975-308_952207b1-7a24-444d-ae1b-2848d883da72
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CYCLOPHOSPHAMIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- ANI Pharmaceuticals, Inc.
- Application
- ANDA207014
- Marketing category
- ANDA
- Marketing start
- 2018-03-20
- Marketing end
- 0000-00-00
- Substance
- CYCLOPHOSPHAMIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Alkylating Activity [MoA],Alkylating Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 43975-308-10 | 43975030810 | 100 CAPSULE in 1 BOTTLE (43975-308-10) | 100 capsule | 2018-03-20 | 0000-00-00 | No | No | Current |