Class III · Low risk
Wal-Fex D
Failed Dissolution Specifications
National Drug Code
Is NDC 0363-1606-30 recalled?
Fexofenadine HCl and Pseudoephedrine HCI · 6 BLISTER PACK in 1 CARTON (0363-1606-30) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Yes — this exact package was recalled
1 FDA recall names the code 0363-1606-30 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
- Fexofenadine HCl and Pseudoephedrine HCI
- Strength
- FEXOFENADINE HYDROCHLORIDE 60 mg/1; PSEUDOEPHEDRINE…
- Form
- Tablet, Extended Release · Oral
- Labeler
- Walgreens Company
- Type
- Human OTC Drug
- Product code
- 0363-1606
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
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