NDC 50090-0293

triamcinolone acetonide 0.25 mg per 1 g cream

Where the pills inside were 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 E. FOUGERA & CO., A division of Nycomed US Inc. names for other drugs.

Apr 13, 2022 · Class II · Mckesson Medical-Surgical Inc. Corporate Office
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 · Fougera Pharmaceuticals Inc.
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

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Generic drug: Triamcinolone Acetonide: every company that makes it
Form: cream, topical
Strength: 0.25 mg per 1 g
Approval: ANDA ANDA085692
On the market since: Mar 9, 1978
Package NDCs: 50090-0293-1
Official label: DailyMed (National Library of Medicine), updated Dec 9, 2023

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?