Bacitracin
- Product NDC
- 0009-0233
- 11-digit product format
- 000090233
- Labeler code
- 0009
- Product ID
- 0009-0233_fca2ebff-656e-4e5a-a635-5eb55ad9a9f1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bacitracin
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR
- Labeler
- Pharmacia & Upjohn Company LLC
- 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 |
|---|
| 0009-0233-01 | 00009023301 | 1 VIAL in 1 CARTON (0009-0233-01) > 10 mL in 1 VIAL | 1 vial | 1948-07-29 | 0000-00-00 | No | No | Current |
| 0009-0233-03 | 00009023303 | 10 VIAL in 1 CARTON (0009-0233-03) > 10 mL in 1 VIAL | 10 vial | 1948-07-29 | 2022-01-31 | No | No | Current |
| 0009-0233-44 | 00009023344 | 1 VIAL in 1 CARTON (0009-0233-44) > 10 mL in 1 VIAL | 1 vial | 1948-07-29 | 0000-00-00 | No | No | Current |
| 0009-0233-45 | 00009023345 | 10 VIAL in 1 CARTON (0009-0233-45) > 10 mL in 1 VIAL | 10 vial | 1948-07-29 | 2022-01-31 | No | No | Current |