Class II · Moderate risk
GloStrips
Failed Impurities/Degradation Specifications: The Active Pharmaceutical Ingredient (API) used in the product is not being manufactured to the current USP monograph in regard to Unspecified Impurities.
National Drug Code
Is NDC 51801-0003-50 recalled?
GloStrips · 300 POUCH in 1 CARTON (51801-003-50) / 1 STRIP in 1 POUCH
Yes — this exact package was recalled
2 FDA recalls name the code 51801-0003-50 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.
1 of these recalls is still ongoing.
- Active ingredient
- Fluorescein Sodium
- Strength
- FLUORESCEIN SODIUM .6 mg/1
- Form
- Strip · Ophthalmic
- Labeler
- Nomax Inc.
- Type
- Human Prescription Drug
- Product code
- 51801-0003
Recalls naming this package
Class III · Low risk
Fluorescein Sodium Ophthalmic Strips USP
Failed Content Uniformity Specifications: The product may not meet finished product release specifications, including the uniformity of dosage due to a packaging degradation related to the adhesive component of the paper pouch that can impact the level of fluorescein present in the strips.
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
- 51801-0004 GloStrips 1
- 51801-0008 Dry Eye Test 1
- 51801-0009 GloStrips 1
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