93/12

Pill imprint 93/12 has been identified as Pantoprazole sodium delayed-release 40 mg.

Pantoprazole is used in the treatment of stomach ulcer; gerd; peptic ulcer; erosive esophagitis; barrett's esophagus (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 subject to the Controlled Substances Act.
See also related documents.

Pantoprazole sodium delayed-release Images

Imprint:
93/12
Strength:
40 mg
Color:
Yellow
Size:
10.00 mm
Shape:
Elliptical / Oval
Availability:
Prescription only
Inactive Ingredients:
calcium carbonate
calcium stearate
D&C Yellow No. 10
aluminum oxide
FD&C Yellow No. 6
hypromelloses
ferrosoferric oxide
ferric oxide yellow
lactose monohydrate
low substituted hydroxypropyl cellulose
methacrylic acid - ethyl acrylate copolymer (1:1) type a
microcrystalline cellulose
polyethylene glycol
shellac
sodium carbonate
stearic acid
magnesium silicate
titanium dioxide
triethyl citrate
propylene glycol
soya lecithin
Drug Class:
Proton pump inhibitors
Pregnancy Category:
B - No proven risk in humans
CSA Schedule:
N - Not a controlled drug
Manufacturer:
Teva Pharmaceuticals USA
National Drug Code (NDC):
00093-0012
Other Manufacturers / Repackagers:
NDC CodeManufacturer / Repackager
18837-0296 Innoviant Pharmacy Inc (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.

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Pantoprazole sodium delayed-release 40 mg 93/12
Pantoprazole sodium delayed-release 40 mg 93/12
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