Clindamycin Hydrochloride

Product NDC
68071-3681
11-digit product format
680713681
Labeler code
68071
Product ID
68071-3681_2a313eb4-4c20-16d2-e063-6394a90ab025
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Clindamycin Hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
NuCare Pharmaceuticals, Inc.
Application
ANDA216957
Marketing category
ANDA
Marketing start
2023-03-10
Substance
CLINDAMYCIN HYDROCHLORIDE
Active strength
150 mg/1
Pharmacologic classes
Decreased Sebaceous Gland Activity [PE], Lincosamide Antibacterial [EPC], Lincosamides [CS], Neuromuscular Blockade [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
T20OQ1YN1WCLINDAMYCIN HYDROCHLORIDE21462-39-5CLINDAMYCIN HYDROCHLORIDE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
68071-3681-4680713681044 CAPSULE in 1 BOTTLE (68071-3681-4) 4 capsule2024-10-08NoNoHistorical
68071-3681-6680713681066 CAPSULE in 1 BOTTLE (68071-3681-6) 6 capsule2024-09-06NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Clindamycin Hydrochloride Capsules, USPNuCare Pharmaceuticals, Inc.2024-12-26HUMAN PRESCRIPTION DRUG LABEL3