Class III ยท Low risk
Clonidine Hydrochloride Tablets
Product mix-up:0.2 mg strength Clonidine Hydrochloride Tablets, USP in a 100-count bottle of 0.3 mg strength Clonidine Hydrochloride Tablets,
National Drug Code
Is NDC 29300-0137-01 recalled?
clonidine hydrochloride · 100 TABLET in 1 BOTTLE, PLASTIC (29300-137-01)
Yes — this exact package was recalled
1 FDA recall names the code 29300-0137-01 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.
- Active ingredient
- clonidine hydrochloride
- Strength
- CLONIDINE HYDROCHLORIDE .3 mg/1
- Form
- Tablet · Oral
- Labeler
- Unichem Pharmaceuticals (USA), Inc.
- Type
- Human Prescription Drug
- Product code
- 29300-0137
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
- 29300-0126 Bisoprolol Fumarate 2
- 29300-0128 Hydrochlorothiazide 2
- 29300-0135 See recall 2
- 29300-0113 Lamotrigine 1
- 29300-0116 topiramate 1
- 29300-0140 Divalproex Sodium 1
Free recall alerts
Know the day your medication is recalled
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