Bleomycin
- Product NDC
- 70121-1567
- 11-digit product format
- 701211567
- Labeler code
- 70121
- Product ID
- 70121-1567_ff4ec56a-242e-4e7b-a7e9-5c8b7892ab12
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bleomycin
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRA-ARTERIAL; INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Amneal Pharmaceuticals LLC
- Marketing category
- UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
- Marketing start
- 2016-06-20
- Marketing end
- 0000-00-00
- Substance
- BLEOMYCIN SULFATE
- Active strength
- 15000 [iU]/1
- Pharmacologic classes
- Cytoprotective Agent [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70121-1567 | BLEOMYCIN INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [AMNEAL PHARMACEUTICALS LLC] | 8 | Legacy NDC | 20231224_38955939-8d1e-4db2-9aed-3bab72ca5f8f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70121-1567-1 | 70121156701 | 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (70121-1567-1) | 2016-06-20 | 0000-00-00 | No | No | Current |