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NDC 00009-0602-25 Cleocin Phosphate 150 mg/mL Details
Cleocin Phosphate 150 mg/mL
Cleocin Phosphate is a INTRAMUSCULAR; INTRAVENOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Pharmacia & Upjohn Company LLC. The primary component is CLINDAMYCIN PHOSPHATE.
MedlinePlus Drug Summary
Clindamycin injection is used to treat certain types of bacterial infections, including infections of the lungs, skin, blood, bones, joints, female reproductive organs, and internal organs. Clindamycin is in a class of medications called lincomycin antibiotics. It works by slowing or stopping the growth of bacteria. Antibiotics such as clindamycin will not work for colds, flu, or other viral infections. Using antibiotics when they are not needed increases your risk of getting an infection later that resists antibiotic treatment.
Related Packages: 00009-0602-25Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Clindamycin Injection
Product Information
| NDC | 00009-0602 |
|---|---|
| Product ID | 0009-0602_9a974170-4735-4211-870d-49df47cb9317 |
| Associated GPIs | 16220020302032 |
| GCN Sequence Number | 009344 |
| GCN Sequence Number Description | clindamycin phosphate VIAL 150 MG/ML INJECTION |
| HIC3 | W1K |
| HIC3 Description | LINCOSAMIDE ANTIBIOTICS |
| GCN | 40843 |
| HICL Sequence Number | 004045 |
| HICL Sequence Number Description | CLINDAMYCIN PHOSPHATE |
| Brand/Generic | Brand |
| Proprietary Name | Cleocin Phosphate |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | clindamycin phosphate |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION, SOLUTION |
| Route | INTRAMUSCULAR; INTRAVENOUS |
| Active Ingredient Strength | 150 |
| Active Ingredient Units | mg/mL |
| Substance Name | CLINDAMYCIN PHOSPHATE |
| Labeler Name | Pharmacia & Upjohn Company LLC |
| Pharmaceutical Class | Decreased Sebaceous Gland Activity [PE], Lincosamide Antibacterial [EPC], Lincosamides [CS], Neuromuscular Blockade [PE] |
| DEA Schedule | n/a |
| Marketing Category | NDA |
| Application Number | NDA050441 |
| Listing Certified Through | 2023-12-31 |
Package
NDC 00009-0602-25 (00009060225)
| NDC Package Code | 0009-0602-25 |
|---|---|
| Billing NDC | 00009060225 |
| Package | 25 VIAL in 1 CARTON (0009-0602-25) / 4 mL in 1 VIAL (0009-0602-04) |
| Marketing Start Date | 2014-04-10 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |