Class II · Moderate risk
Ibuprofen Tablets USP 600 mg
CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being recalled due to complaints of odor related to CGMP deficiencies.
National Drug Code
Is NDC 49483-0603-50 recalled?
Ibuprofen · 500 TABLET, FILM COATED in 1 BOTTLE (49483-603-50)
Yes — this exact package was recalled
2 FDA recalls name the code 49483-0603-50 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
- Ibuprofen
- Strength
- IBUPROFEN 600 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Time Cap Laboratories, INC
- Type
- Human Prescription Drug
- Product code
- 49483-0603
Recalls naming this package
Class II · Moderate risk
Ibuprofen Tablets
Presence of foreign tablets/capsules: Ibuprofen Tablets USP, 600 mg bottles were found to contain some Ibuprofen Tablets USP 800 mg.
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
- 49483-0623 Metformin Hydrochloride Extended Release 3
- 49483-0600 Ibuprofen 1
- 49483-0601 Ibuprofen 1
- 49483-0602 Ibuprofen 1
- 49483-0604 Ibuprofen 1
- 49483-0624 Metformin Hydrochloride Extended Release 1
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