93/12 (Pantoprazole sodium delayed-release 40 mg)
Pill imprint 93/12 has been identified as Pantoprazole sodium delayed-release 40 mg.
Pantoprazole is used in the treatment of barrett's esophagus; gerd; dumping syndrome; erosive esophagitis; duodenal ulcer (and more), and belongs to the drug class proton pump inhibitors. There is no proven risk in humans during pregnancy. Pantoprazole 40 mg is not a controlled substance under the Controlled Substance Act (CSA).
- 40 mg
- 10.00 mm
- Elliptical / Oval
- Prescription only
- Drug Class:
- Proton pump inhibitors
- Pregnancy Category:
- B - No proven risk in humans
- CSA Schedule:
- Not a controlled drug
- Teva Pharmaceuticals USA
- National Drug Code (NDC):
- Inactive Ingredients:
- calcium carbonate
D&C Yellow No. 10
FD&C Yellow No. 6
hypromellose 2910 (15 mPa.s)
ferric oxide yellow
low substituted hydroxypropyl cellulose
methacrylic acid - ethyl acrylate copolymer (1:1) type a
polyethylene glycol 4000
|NDC Code||Manufacturer / Repackager|
|54868-5846||Physicians Total Care Inc (repackager)|
|68071-0782||Nucare Pharmaceuticals Inc (repackager)|
|66336-0405||Dispensing Solutions Inc. (repackager)|
Note: Inactive ingredients may vary.
More about pantoprazole
- Pantoprazole delayed-release tablets
- Pantoprazole suspension
- Pantoprazole (Advanced Reading)
- Pantoprazole Intravenous (Advanced Reading)
Related treatment guides
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