NDC 0406-8320 – Morphine Sulfate

Morphine Sulfate 200 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug DEA schedule CII

Product NDC0406-8320

Product details

Brand name
Morphine Sulfate
Generic name
Morphine Sulfate
Labeler
SpecGx LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA076438
Marketed since
July 3, 2003
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
0406-8320-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0406-8320-01)Jul 3, 2003

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