Clindamycin in 5 Percent Dextrose
- Product NDC
- 0781-9220
- 11-digit product format
- 007819220
- Labeler code
- 0781
- Product ID
- 0781-9220_9ab06e2f-6a2f-41a5-8386-81d3aba03cfc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clindamycin in 5 Percent Dextrose
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Sandoz Inc
- Application
- ANDA201692
- Marketing category
- ANDA
- Marketing start
- 2014-03-01
- Marketing end
- 0000-00-00
- Substance
- CLINDAMYCIN
- Active strength
- 6 mg/mL
- Pharmacologic classes
- Decreased Sebaceous Gland Activity [PE], Lincosamide Antibacterial [EPC], Lincosamides [CS], Neuromuscular Blockade [PE]
- 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 |
|---|
| 0781-9220-09 | 00781922009 | 24 BAG in 1 CARTON (0781-9220-09) > 50 mL in 1 BAG (0781-9220-91) | 24 bag | 2014-03-01 | 0000-00-00 | No | No | Current |