Clindamycin Hydrochloride

Product NDC
42292-018
11-digit product format
422920018
Labeler code
42292
Product ID
42292-018_9aee45ba-92b5-0837-e053-2a95a90ad834
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Clindamycin Hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
Mylan Institutional Inc.
Application
ANDA065442
Marketing category
ANDA
Marketing start
2016-09-22
Marketing end
2021-01-31
Substance
CLINDAMYCIN HYDROCHLORIDE
Active strength
150 mg/1
Pharmacologic classes
Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [CS]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
42292-018-01EA - Each42292-018113f2b8c-fe69-4d30-8e8e-ab76cd17712512016-11-08
42292-018-20EA - Each42292-0189d9518b6-adf6-45ff-9f3b-503d77c96d1012016-11-08