Class I · High risk
Methocarbamol 500mg Tablet
Labeling: Label Error on Declared Strength; Bottles labeled as Methocarbamol 500 mg Tablets actually contain Methocarbamol 750 mg Tablets
National Drug Code
Is NDC 71335-1795-07 recalled?
Methocarbamol · 90 TABLET in 1 BOTTLE (71335-1795-7)
Yes — this exact package was recalled
1 FDA recall names the code 71335-1795-07 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
- Methocarbamol
- Strength
- METHOCARBAMOL 500 mg/1
- Form
- Tablet · Oral
- Labeler
- Bryant Ranch Prepack
- Type
- Human Prescription Drug
- Product code
- 71335-1795
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
- 71335-0567 Valsartan 1
- 71335-1767 Butalbital, Acetaminophen, Caffeine 1
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.