Herceptin
- Product NDC
- 50242-134
- 11-digit product format
- 502420134
- Labeler code
- 50242
- Product ID
- 50242-134_68805c84-fc83-4bc6-9311-2fec065cc3b8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trastuzumab
- Dosage form
- KIT
- Labeler
- Genentech, Inc.
- Application
- BLA103792
- Marketing category
- BLA
- Marketing start
- 1998-09-25
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50242-134-68 | EA - Each | 50242-134 | c507fcab-bf09-4dc0-b148-e58561308db9 | 1 | 2012-07-24 |