Bacitracin
- Product NDC
- 0009-0234
- 11-digit product format
- 000090234
- Labeler code
- 0009
- Product ID
- 0009-0234_f1fd5f9f-1287-4422-8936-0429443b3541
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bacitracin
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR
- Labeler
- Pharmacia and Upjohn Company LLC
- Application
- ANDA060733
- Marketing category
- ANDA
- Marketing start
- 1948-07-29
- Marketing end
- 2021-03-31
- Substance
- BACITRACIN
- Active strength
- 5000 [USP'U]/mL
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0009-0234-02 | 00009023402 | 10 VIAL in 1 CARTON (0009-0234-02) > 1 mL in 1 VIAL | 10 vial | 1948-07-29 | 2021-03-31 | No | No | Current |