Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 63629-1088-01 recalled?

Morphine sulfate · 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-1088-1)

Yes — this exact package was recalled

1 FDA recall names the code 63629-1088-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

Active ingredient
morphine sulfate
Strength
MORPHINE SULFATE 30 mg/1
Form
Tablet, Film Coated, Extended Release · Oral
Labeler
Bryant Ranch Prepack
Type
Human Prescription Drug · DEA CII
Product code
63629-1088

Recalls naming this package

Class I ยท High risk

Morphine Sulfate extended-Release Tablets

Labeling: Label Mix-up: bottles labeled as Morphine Sulfate 60 mg Extended-Release tablets contain Morphine Sulfate 30 mg Extended-Release tablets and bottles labeled as Morphine Sulfate 30 mg Extended-Release tablets may contain Morphine Sulfate 60 mg Extended-Release tablets.

Terminated Labeling / mix-up Bryant Ranch Prepack, Inc. D-1187-2022

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.

Other recalled products from this labeler