Class III · Low risk
Butalbital
Labeling: Not Elsewhere Classified: the controlled substance classification "CIII" is missing on the label
National Drug Code
Is NDC 63629-8392-04 recalled?
Butalbital, Acetaminophen, and Caffeine · 90 TABLET in 1 BOTTLE (63629-8392-4)
Yes — this exact package was recalled
1 FDA recall names the code 63629-8392-04 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.
1 of these recalls is still ongoing.
- Active ingredient
- Butalbital, Acetaminophen, and Caffeine
- Strength
- BUTALBITAL 50 mg/1; ACETAMINOPHEN 325 mg/1; CAFFEINE 40 mg/1
- Form
- Tablet · Oral
- Labeler
- Bryant Ranch Prepack
- Type
- Human Prescription Drug · DEA CIII
- Product code
- 63629-8392
Recalls naming this package
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
- 63629-1064 Spironolactone 1
- 63629-1067 Spironolactone 1
- 63629-1088 Morphine sulfate 1
- 63629-1089 Morphine sulfate 1
- 63629-3324 Venlafaxine 1
- 63629-6905 See recall 1
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