Class III ยท Low risk
Diazepam Rectal Gel
Labeling: Incorrect or Missing Lot and/or Exp Date: Product distributed without a lot number or expiration date on the outer carton.
National Drug Code
Is NDC 68682-0650-20 recalled?
Diazepam · 2 SYRINGE, PLASTIC in 1 PACKAGE (68682-650-20) / .5 mL in 1 SYRINGE, PLASTIC
Yes — this exact package was recalled
1 FDA recall names the code 68682-0650-20 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
- Diazepam
- Strength
- DIAZEPAM 2.5 mg/.5mL
- Form
- Gel · Rectal
- Labeler
- Oceanside Pharmaceuticals
- Type
- Human Prescription Drug · DEA CIV
- Product code
- 68682-0650
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
- 68682-0170 See recall 2
- 68682-0270 See recall 1
- 68682-0409 See recall 1
- 68682-0521 See recall 1
- 68682-0991 See recall 1
Free recall alerts
Know the day your medication is recalled
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