Class II · Moderate risk
Betamethasone Dipropionate Ointment USP
CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc.is discontinuing its stability study program.
National Drug Code
Is NDC 63739-0996-15 recalled?
Betamethasone Dipropionate Ointment USP
Yes — this exact package was recalled
1 FDA recall names the code 63739-0996-15 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.
This code is not in the current FDA NDC directory — usual for a product that has since been discontinued or repackaged. The details below come from the recall notices themselves.
Recalls naming this package
Class III · Low risk
Betamethasone Dipropionate Ointment USP
Failed Impurities/ Degradation Specifications - OOS for know impurity Betamethasone 17- propionate.
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
- 63739-0997 Lidocaine Hydrochloride 3
- 63739-0053 See recall 2
- 63739-0434 See recall 2
- 63739-0549 See recall 2
- 63739-0998 See recall 2
- 63739-0014 See recall 1
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