NDC 76420-760
Lidolog Kit 10 mg per 1 mL / 20 mg per 1 mL / 40 mg per 1 mL kit
On the label: Asclemed USA, Inc..
Where it's 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.
Recalls
- Jul 15, 2026 · Class III · Asclemed USA Inc.
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
Lots: Lot: 070126X1, Exp. 12/31/2027. - May 18, 2026 · Class III · Eugia US LLC
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
Lots: Lot, expiry: Lot 3LC26029A, exp Feb-2029; Lot 3LC26031A, exp Mar-2029
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Iodine and Lidocaine and Triamcinolone Acetonide: every company that makes it
- Form
- kit, epidural; infiltration; intra-articular; intramuscular; topical
- Strength
- 10 mg per 1 mL / 20 mg per 1 mL / 40 mg per 1 mL
- Approval
- unapproved drug other
- On the market since
- May 10, 2018
- Package NDCs
55150-164-0267777-419-0270121-1049-576420-760-01- Official label
- DailyMed (National Library of Medicine), updated Oct 5, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?