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 AbbVie Inc. names for other drugs.
Recalls
- Jan 13, 2017 · Class II · AbbVie Inc.
Failed Stability Specifications: confirmed out of specification results obtained during refrigerated material stability testing indicating that drug may settle within drug cassettes nearing the end of their refrigerated shelf-life
Lots: Lots: 1055692, Expiration Date (Frozen) 06/01/2018 1057881, Expiration Date (Frozen) 06/02/2018 1060138, Expiration Date (Frozen) 06/13/2018 1060140, Expiration Date (Frozen) 06/15/2018 1061258, Expiration Date (Frozen) 06/17/2018 1061262, Expiration Date (Frozen) 06/30/2018 1063033, Expirat…
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Carbidopa and Levodopa: every company that makes it
- Form
- suspension, enteral
- Strength
- 20 mg per 1 mL / 4.63 mg per 1 mL
- Approval
- NDA NDA203952
- On the market since
- Jan 15, 2015
- Package NDCs
0074-3012-07- Official label
- DailyMed (National Library of Medicine), updated Mar 19, 2026
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