NDC 80425-0533
Marbeta L Kit 6 ingredients kit
On the label: Advanced Rx Pharmacy of Tennessee, LLC. It's repackaged: Advanced Rx Pharmacy of Tennessee, LLC rebottles it from Asclemed USA, Inc.'s NDC 76420-782.
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 Asclemed USA, Inc. names for other drugs.
Repackaging site
- Advanced Rx Pharmacy of Tennessee, LLC, Nashville, TN, United States · repackages it
Recalls
- Mar 28, 2019 · Class I · Aurobindo Pharma USA Inc.
Presence of Particulate Matter: One vial was found to contain a hair.
Lots: Lot #: CLC180117, Exp. June 2021
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Betamethasone Sodium Phosphate, Betamethasone Acetate, Lidocaine Hydrochloride, : every company that makes it
- Form
- kit, epidural; infiltration; intra-articular; intralesional; intramuscular; topical
- Strength
- 6 ingredients
- Approval
- unapproved drug other
- On the market since
- Jun 2, 2025
- Package NDCs
0409-1159-180517-0720-0155150-162-0567777-419-0280425-0533-1- Official label
- DailyMed (National Library of Medicine), updated Jun 2, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?