NDC 0168-0002

triamcinolone acetonide 5 mg per 1 g cream

Where it's made

This label doesn't name the factory that makes the drug. Companies aren't required to print it on the label. The manufacturer's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants E. FOUGERA & CO., A division of Nycomed US Inc. uses for other drugs.

Apr 13, 2022 · Class II · Terminated
cGMP deviations: Temperature abuse
Lots: McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer.
Jan 29, 2014 · Class III · Terminated
Labeling: Label Error on Declared Strength: There is a misprint on the end flap which read 01% rather than 0.1%.
Lots: Lot #: 485P, 486P, 487P, 488P, Exp 06/15; 638P, 639P, 640P, Exp 07/15; 753P, 754P, 755P, Exp 08/15; 898P, 756P, 757P, 758P, 899P, 900P, 901P, 902P, Exp 09/15

Generic drug: Triamcinolone Acetonide: see every company that makes it
Form: cream, topical
Strength: 5 mg per 1 g
Approval: ANDA ANDA085692
On the market since: Mar 9, 1978
Package NDCs: 0168-0002-15
Official label: DailyMed (National Library of Medicine), updated Jan 28, 2026

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