0008-0607 : Pantoprazole 40 mg (As Pantoprazole Sodium Sesquihydrate 45.1 mg) Delayed Release Tablet

NDC:	0008-0607
Labeler:	Wyeth Pharmaceuticals Inc., a Subsidiary of Pfizer Inc.
Product Type:	Human Prescription Drug
Drug Name:	Pantoprazole Sodium Delayed-release
Dosage Form:	Oral Tablet, Delayed Release
Application #:	NDA020987
Rev. Date:	Jan 31, 2008

Appearance:

Markings:	P;40 OR PROTONIX
Shapes:	Oval
Colors:	Yellow
Size (mm):	12
Segments: ^*	1
^* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

P 40 OR PROTONIX: (0008-0607) Pantoprazole 40 mg (As Pantoprazole Sodium Sesquihydrate 45.1 mg) Delayed Release Tablet by Wyeth Pharmaceuticals Inc., a Subsidiary of Pfizer Inc.

The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.

NDC Package Codes:

0008-0607-01: 90 TABLET, DELAYED RELEASE IN 1 BOTTLE (0008‑0607‑01)
0008-0607-04: 100 BLISTER PACK IN 1 CARTON (0008‑0607‑04) > 1 TABLET, DELAYED RELEASE IN 1 BLISTER PACK

Active Ingredients:

Pantoprazole Sodium

Dosage Strength:

40 mg

Inactive Ingredients:

Calcium Stearate
Crospovidone
Ferric Oxide Yellow
Mannitol
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 2208 (100 Mpa.s)

Pharmaceutical Classes:

Proton Pump Inhibitor [EPC]
Proton Pump Inhibitors [MoA]

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.