Bacitracin
- Product NDC
- 0009-0241
- 11-digit product format
- 000090241
- Labeler code
- 0009
- Product ID
- 0009-0241_296ac9fa-fbf1-4577-9686-4793d62bcb6e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bacitracin
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR
- Labeler
- Pharmacia and Upjohn Company
- Application
- ANDA060733
- Marketing category
- ANDA
- Marketing start
- 1948-07-29
- Marketing end
- 2022-01-31
- Substance
- BACITRACIN A
- Active strength
- 5000 [USP'U]/mL
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0009-0241-01 | 00009024101 | 1 VIAL in 1 CARTON (0009-0241-01) > 1 mL in 1 VIAL | 1 vial | 1948-07-29 | 0000-00-00 | No | No | Current |
| 0009-0241-10 | 00009024110 | 10 VIAL in 1 CARTON (0009-0241-10) > 1 mL in 1 VIAL | 10 vial | 1948-07-29 | 2022-01-31 | No | No | Current |