Colistimethate Sodium
- Product NDC
- 14789-201
- 11-digit product format
- 147890201
- Labeler code
- 14789
- Product ID
- 14789-201_7792cc09-02f8-47a4-a948-79ff051bff71
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Colistimethate Sodium
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Nexus Pharmaceuticals Inc
- Application
- ANDA065177
- Marketing category
- ANDA
- Marketing start
- 2021-12-06
- Marketing end
- 0000-00-00
- Substance
- COLISTIMETHATE SODIUM
- Active strength
- 150 mg/1
- Pharmacologic classes
- Polymyxin-class Antibacterial [EPC], Polymyxins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 14789-201-05 | 14789020105 | 10 VIAL in 1 CARTON (14789-201-05) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (14789-201-07) | 10 vial | 2021-12-06 | 0000-00-00 | No | No | Current |