50090-1804 : Lansoprazole 30 mg Oral Capsule, Delayed Release

NDC:	50090-1804
Labeler:	A-s Medication Solutions
Product Type:	Human Prescription Drug
Drug Name:	Lansoprazole
Dosage Form:	Oral Capsule, Delayed Release
Application #:	ANDA091509
Rev. Date:	Dec 15, 2014

Appearance:

Markings:	924;924
Shapes:	Capsule
Colors:	Pink / Black
Size (mm):	19
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:

50090-1804-0: 30 CAPSULE, DELAYED RELEASE IN 1 BOTTLE (50090‑1804‑0)
50090-1804-1: 90 CAPSULE, DELAYED RELEASE IN 1 BOTTLE (50090‑1804‑1)

Active Ingredients:

Lansoprazole

Dosage Strength:

30 mg

Inactive Ingredients:

Magnesium Carbonate
Hydroxypropyl Cellulose, Low Substituted
Hypromellose 2910 (5 Mpa.s)
Starch, Corn
Sucrose
Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
Polyethylene Glycol 6000
Talc
Titanium Dioxide
Polysorbate 80
Gelatin
Sodium Lauryl Sulfate
Fd&c Blue No. 1
D&c Red No. 28
Fd&c Red No. 40
Shellac
Alcohol
Isopropyl Alcohol
Butyl Alcohol
Propylene Glycol
Ammonia
Potassium Hydroxide
Water

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.