0615-7916 : Pantoprazole Sodium 20 mg Oral Tablet, Delayed Release

NDC:	0615-7916
Labeler:	Ncs Healthcare of Ky, Inc Dba Vangard Labs
Product Type:	Human Prescription Drug
Drug Name:	Pantoprazole Sodium
Dosage Form:	Oral Tablet, Delayed Release
Application #:	ANDA077056
Rev. Date:	Dec 21, 2007

Appearance:

Markings:	93;11
Shapes:	Oval
Colors:	Yellow
Size (mm):	8
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.

93 11: (0093-0011) Pantoprazole Sodium 20 mg Oral Tablet, Delayed Release by Ncs Healthcare of Ky, Inc Dba Vangard Labs

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:

0615-7916-39: 30 TABLET, DELAYED RELEASE IN 1 BLISTER PACK (0615‑7916‑39)

Active Ingredients:

Pantoprazole Sodium

Dosage Strength:

20 mg

Inactive Ingredients:

Calcium Carbonate
Calcium Stearate
D&c Yellow No. 10
Aluminum Oxide
Fd&c Yellow No. 6
Hypromellose 2910 (15 Mpa.s)
Ferrosoferric Oxide
Ferric Oxide Yellow
Lactose Monohydrate
Hydroxypropyl Cellulose, Low Substituted
Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
Cellulose, Microcrystalline
Polyethylene Glycol 4000
Propylene Glycol
Shellac
Sodium Carbonate
Stearic Acid
Talc
Titanium Dioxide
Triethyl Citrate

Pharmaceutical Classes:

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

NDC QR Code

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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.