NDC 25021-315
Phenylephrine Hydrochloride 10 mg per 1 mL injection, solution
On the label: Sagent Pharmaceuticals.
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 Sagent Pharmaceuticals names for other drugs.
Recalls
- Mar 11, 2021 · Class II · Sagent Pharmaceuticals Inc
Lack of Assurance of Sterility: customer complaints of loose crimped vial overseals which may result in a non-sterile product.
Lots: Lots: PHT8IB2, PHT9IB2, exp 08/2022; PHT1JB2, exp 09/2022
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Phenylephrine: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 10 mg per 1 mL
- Approval
- ANDA ANDA209967
- On the market since
- Oct 15, 2020
- Package NDCs
25021-315-0125021-315-9825021-315-99- Official label
- DailyMed (National Library of Medicine), updated Jul 10, 2020
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