Bacitracin
- Product NDC
- 70594-026
- 11-digit product format
- 705940026
- Labeler code
- 70594
- Product ID
- 70594-026_edf20b28-c044-4261-9cd9-bf0164e42b9c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bacitracin
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR
- Labeler
- Xellia Pharmaceuticals USA LLC
- Application
- ANDA203177
- Marketing category
- ANDA
- Marketing start
- 2018-10-01
- Marketing end
- 2023-03-31
- Substance
- BACITRACIN
- Active strength
- 50000 [USP'U]/1
- Pharmacologic classes
- Decreased Cell Wall Synthesis & Repair [PE]
- 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 |
|---|
| 70594-026-01 | 70594002601 | 1 VIAL, GLASS in 1 CARTON (70594-026-01) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS | 2018-10-01 | 0000-00-00 | No | No | Current |
| 70594-026-02 | 70594002602 | 10 VIAL, GLASS in 1 CARTON (70594-026-02) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS | 2018-10-01 | 0000-00-00 | No | No | Current |
| 70594-026-04 | 70594002604 | 10 VIAL, GLASS in 1 CARTON (70594-026-04) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS (70594-026-03) | 2019-06-14 | 0000-00-00 | No | No | Current |