NDC 63187-214
Triamcinolone Acetonide 0.25 mg per 1 g cream
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from E. FOUGERA & CO., A division of Nycomed US Inc.'s NDC 0168-0003.
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.
Repackaging site
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels it
Recalls
- 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.
Product details
- 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
63187-214-80- Official label
- DailyMed (National Library of Medicine), updated Dec 1, 2019
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?