NDC 27808-082 – Morphine Sulfate

Morphine Sulfate 20 mg/mL · Solution · Oral

Human Prescription Drug DEA schedule CII 1 recall

Product NDC27808-082

Product details

Brand name
Morphine Sulfate
Generic name
Morphine Sulfate
Labeler
Cranbury Pharmaceuticals, LLC
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA203518
Marketed since
September 21, 2015
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
27808-082-011 BOTTLE, UNIT-DOSE in 1 CARTON (27808-082-01) / 30 mL in 1 BOTTLE, UNIT-DOSESep 21, 2015
27808-082-021 BOTTLE, UNIT-DOSE in 1 CARTON (27808-082-02) / 120 mL in 1 BOTTLE, UNIT-DOSESep 21, 2015

Recalls mentioning this NDC

Other Morphine Sulfate products