Pill Identifier Protonix Delayed-release - NDC 0008-0841
Pantoprazole Sodium
Product Code 0008-0841
Protonix Delayed-release by Wyeth Pharmaceuticals Llc, A Subsidiary Of Pfizer Inc. is a yellow oval tablet delayed release about 12 mm in size, imprinted with protonix. The product is a human prescription drug with active ingredient(s) pantoprazole sodium.
Protonix Delayed-release
Active Ingredient(s): Pantoprazole Sodium
Inactive Ingredient(s):
- CALCIUM STEARATE
- CROSPOVIDONE (15 MPA.S AT 5%)
- MANNITOL
- FERRIC OXIDE YELLOW
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
- POLYSORBATE 80
- POVIDONE K25
- POVIDONE K90
- PROPYLENE GLYCOL
- SODIUM CARBONATE
- SODIUM LAURYL SULFATE
- TITANIUM DIOXIDE
- TRIETHYL CITRATE
- HYPROMELLOSE 2910 (6 MPA.S)
Wyeth Pharmaceuticals Llc, A Subsidiary Of Pfizer Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Delayed Release
- Yellow (C48330)
Product Packages
NDC Package Code | Package Description |
---|---|
0008-0841-81 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE |
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Pill Identification data last updated on: December, 2018
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