Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Akorn names for other drugs.
Recalls
- Apr 19, 2024 · Class II · Nomax Inc
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.
Lots: Lot #: 14776, Exp. 05/31/2024. - Mar 24, 2015 · Class III · Nomax Inc
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.
Lots: 1) FUL-GLO Lot: 8980, Exp 10/15; 9081, Exp 01/16; 9088, Exp 02/16; 9128 and 9158, Exp 03/16; 2) Pro Glo Lot: 9082, Exp 01/17
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Fluorescein: every company that makes it
- Form
- strip
- Strength
- 1 mg
- Approval
- Unapproved drug other
- On the market since
- Jun 1, 2004
- Package NDCs
17478-404-01- Official label
- DailyMed (National Library of Medicine), updated Sep 12, 2022
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?