NDC 63304-451 – Morphine sulfate

Morphine Sulfate 30 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug DEA schedule CII 1 recall

Product NDC63304-451

Product details

Brand name
Morphine sulfate
Generic name
morphine sulfate
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA078761
Marketed since
May 11, 2012
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Morphine Sulfate →

Package NDC codes (3)

Package NDCDescriptionSince
63304-451-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-451-01)May 11, 2012
63304-451-0310 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-451-03)May 11, 2012
63304-451-05500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-451-05)May 11, 2012

Recalls mentioning this NDC

Other Morphine Sulfate products