Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 0069-4200-30 recalled?

Viagra · 30 TABLET, FILM COATED in 1 BOTTLE (0069-4200-30)

Yes — this exact package was recalled

1 FDA recall names the code 0069-4200-30 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
sildenafil citrate
Strength
SILDENAFIL CITRATE 25 mg/1
Form
Tablet, Film Coated · Oral
Labeler
Pfizer Laboratories Div Pfizer INC
Type
Human Prescription Drug
Product code
0069-4200

Recalls naming this package

Class II ยท Moderate risk

Sildenafil Citrate

Labeling: Label Mixup: SILDENAFIL CITRATE, Tablet, 25 mg may have potentially been mislabeled as the following drug: PHENobarbital/ HYOSCYAMINE/ ATROPINE/ SCOPOLAMINE, Tablet, 16.2 mg/0.1037 mg/0.0194 mg/0.0065 mg, NDC 66213042510, Pedigree: W003640, EXP: 6/25/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-804-2014

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