Clindamycin Phosphate

Product NDC
72611-642
11-digit product format
726110642
Labeler code
72611
Product ID
72611-642_4ffd5cec-03a6-4531-b8d5-b6e262ee4e3a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
clindamycin phosphate
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Labeler
ALMAJECT, INC.
Application
NDA050441
Marketing category
NDA
Marketing start
1972-10-02
Marketing end
0000-00-00
Substance
CLINDAMYCIN PHOSPHATE
Active strength
150 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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72611-642-01ML - Milliliter72611-64209c5fb92-9ff9-4dad-930e-469668b4edf712019-11-12
72611-642-25ML - Milliliter72611-642221f1b35-b3a1-4e90-a45e-2f994840658912019-11-12

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72611-642-257261106422525 VIAL in 1 CARTON (72611-642-25) > 6 mL in 1 VIAL (72611-642-01) 25 vial2019-06-300000-00-00NoNoCurrent