NDC 21695-368
Pilocarpine Hydrochloride 10 mg per 1 mL solution/ drops
On the label: Rebel Distributors Corp... It's repackaged: Rebel Distributors Corp.. rebottles it from Sandoz Inc.'s NDC 61314-203.
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 Sandoz Inc. names for other drugs.
Recalls
- Mar 22, 2017 · Class III · Novartis Pharmaceuticals Corp.
Failed Impurities/Degradation Specifications.
Lots: Lot #: 244660F, Exp. FEB 2018
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Pilocarpine: every company that makes it
- Form
- solution/ drops
- Strength
- 10 mg per 1 mL
- Approval
- NDA NDA200890
- On the market since
- Jun 22, 2010
- Package NDCs
21695-368-01- Official label
- DailyMed (National Library of Medicine), updated Mar 15, 2011
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?