NDC 0008-0923
ProtonixI.V. 40 mg per 10 mL injection, powder, for solution
On the label: Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc..
Where it's made
This label doesn't name the factory that makes the drug (it lists 1 site that labels it). 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 Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. names for other drugs.
Recalls
- Nov 22, 2016 · Class III · Pfizer Inc.
Subpotent Drug: Out of Specification (OOS) for potency at the 6-month stability time point.
Lots: Lot #: A) a) 325449, Exp 12/16; b) N97969, N69175, N69177, Exp 03/17; N95727, Exp 04/17; B) M51076, Exp 11/16; and C) a) 317364, Exp 11/16; b) N73763, Exp 03/17
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Pantoprazole: every company that makes it
- Form
- injection, powder, for solution, intravenous
- Strength
- 40 mg per 10 mL
- Approval
- NDA NDA020988
- On the market since
- May 1, 2001
- Package NDCs
0008-0923-510008-0923-550008-0923-60- Official label
- DailyMed (National Library of Medicine), updated Dec 22, 2025
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