Busulfan
- Product NDC
- 60505-6177
- 11-digit product format
- 605056177
- Labeler code
- 60505
- Product ID
- 60505-6177_a0b0bc32-8fc8-8c09-04bf-6a751c60360e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- busulfan
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Apotex Corp.
- Application
- ANDA210448
- Marketing category
- ANDA
- Marketing start
- 2019-08-19
- Marketing end
- 2023-01-31
- Substance
- BUSULFAN
- Active strength
- 6 mg/mL
- 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 |
|---|
| 60505-6177-8 | 60505617708 | 8 VIAL, SINGLE-DOSE in 1 CARTON (60505-6177-8) > 10 mL in 1 VIAL, SINGLE-DOSE (60505-6177-0) | 2019-08-19 | 2023-01-31 | No | No | Current |