NDC 63304-693 – Clindamycin hydrochloride

Clindamycin Hydrochloride 300 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

Product NDC63304-693

Product details

Brand name
Clindamycin hydrochloride
Generic name
Clindamycin hydrochloride
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA065061
Marketed since
March 23, 2001
Listing expires
December 31, 2027
Pharmacologic class
Lincosamide Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Clindamycin Hydrochloride →

Package NDC codes (5)

Package NDCDescriptionSince
63304-693-01100 CAPSULE in 1 BOTTLE (63304-693-01)Mar 23, 2001
63304-693-0310 CAPSULE in 1 BOTTLE (63304-693-03)Mar 23, 2001
63304-693-05500 CAPSULE in 1 BOTTLE (63304-693-05)Mar 23, 2001
63304-693-1616 CAPSULE in 1 BOTTLE (63304-693-16)Mar 23, 2001
63304-693-77100 CAPSULE in 1 CARTON (63304-693-77)Mar 23, 2001

Recalls mentioning this NDC

Other Clindamycin Hydrochloride products