50090-2739 : Lansoprazole 15 mg Oral Capsule, Delayed Release

NDC:	50090-2739
Labeler:	A-s Medication Solutions
Product Type:	Human Prescription Drug
Drug Name:	Lansoprazole
Dosage Form:	Oral Capsule, Delayed Release
Application #:	ANDA201921
Rev. Date:	Dec 18, 2012

Appearance:

Markings:	NATCO;15
Shapes:	Capsule
Colors:	Green / Pink
Size (mm):	16
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.

NDC Package Codes:

50090-2739-0: 30 CAPSULE, DELAYED RELEASE IN 1 BOTTLE (50090‑2739‑0)

Active Ingredients:

Lansoprazole

Dosage Strength:

15 mg

Inactive Ingredients:

Acetone
Hypromellose, Unspecified
Isopropyl Alcohol
Magnesium Carbonate
Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
Polyethylene Glycol 4000
Polysorbate 80
Sucrose
Starch, Corn
Talc
Titanium Dioxide
D&c Red No. 28
Fd&c Blue No. 1
Fd&c Green No. 3
Fd&c Red No. 40
Gelatin, Unspecified
Water
Ammonia
Potassium Hydroxide
Propylene Glycol
Shellac /

Pharmaceutical Classes:

Proton Pump Inhibitor [EPC]
Proton Pump Inhibitors [MoA]
Inhibition Gastric Acid Secretion [PE]

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.