Clindamycin Hydrochloride

Product NDC

50268-181

11-digit product format

502680181

Labeler code

50268

Product ID

50268-181_652e9814-786f-2962-e053-2991aa0a67d7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Clindamycin Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

AvPAK

Application

ANDA065442

Marketing category

ANDA

Marketing start

2014-07-15

Marketing end

0000-00-00

Substance

CLINDAMYCIN HYDROCHLORIDE

Active strength

300 mg/1

Pharmacologic classes

Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record