Colistimethate
- Product NDC
- 42023-131
- 11-digit product format
- 420230131
- Labeler code
- 42023
- Product ID
- 42023-131_b09e4e14-6227-4c6a-9a90-ec71675b0a3a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- colistimethate sodium
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Par Pharmaceutical, Inc.
- Application
- NDA050108
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2012-06-01
- Marketing end
- 0000-00-00
- Substance
- COLISTIMETHATE SODIUM
- Active strength
- 150 mg/2mL
- Pharmacologic classes
- Polymyxin-class Antibacterial [EPC],Polymyxins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 42023-131-01 | 42023013101 | 1 VIAL in 1 CARTON (42023-131-01) > 2 mL in 1 VIAL | 1 vial | 2012-06-01 | 0000-00-00 | No | No | Current |
| 42023-131-06 | 42023013106 | 6 VIAL in 1 CARTON (42023-131-06) > 2 mL in 1 VIAL | 6 vial | 2012-06-01 | 0000-00-00 | No | No | Current |