Class III · Low risk
Glycopyrrolate Tablets
Failed Impurities/Degradation Specifications
National Drug Code
Is NDC 13107-0014-01 recalled?
Glycopyrrolate · 100 TABLET in 1 BOTTLE (13107-014-01)
Yes — this exact package was recalled
3 FDA recalls name the code 13107-0014-01 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
- Glycopyrrolate
- Strength
- GLYCOPYRROLATE 1 mg/1
- Form
- Tablet · Oral
- Labeler
- Aurolife Pharma LLC
- Type
- Human Prescription Drug
- Product code
- 13107-0014
Recalls naming this package
Class II · Moderate risk
Glycopyrrolate Tablets
Failed Impurities/Degradation Specifications
Class II · Moderate risk
Glycopyrrolate Tablets
Presence of Foreign Substance: Complaint for pieces of glass discovered in a sealed bottle which came from equipment within the packaging room.
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
- 13107-0031 Mirtazapine 2
- 13107-0059 Acetaminophen and Codeine Phosphate 2
- 13107-0001 Mirtazapine 1
- 13107-0046 Oxycodone and Acetaminophen 1
- 13107-0058 Acetaminophen and Codeine Phosphate 1
- 13107-0060 Acetaminophen and Codeine Phosphate 1
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