62175-515 : Lansoprazole 24 Hr 15 mg Oral Capsule, Delayed Release
| NDC: | 62175-515 |
| Labeler: | Lannett Company, Inc.. |
| Product Type: | Human OTC Drug |
| Drug Name: |  Lansoprazole 24 Hr |
| Dosage Form: | Oral Capsule, Delayed Release |
| Application #: | ANDA207157 |
| Rev. Date: |
Appearance:
| Markings: | KU;515 |
| Shapes: |
Capsule |
| Colors: |
 Green /
 White |
| 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:
- 62175-515-12: 2 BOTTLE IN 1 PACKAGE, COMBINATION (62175‑515‑12) > 14 CAPSULE, DELAYED RELEASE IN 1 BOTTLE
- 62175-515-24: 1 BOTTLE IN 1 CARTON (62175‑515‑24) > 14 CAPSULE, DELAYED RELEASE IN 1 BOTTLE
- 62175-515-52: 3 BOTTLE IN 1 PACKAGE, COMBINATION (62175‑515‑52) > 14 CAPSULE, DELAYED RELEASE IN 1 BOTTLE
Active Ingredients:
- Lansoprazole
Dosage Strength:
- 15 mg
Inactive Ingredients:
- Hydroxide Ion
- Ferrosoferric Oxide
- Butyl Alcohol
- Alcohol
- Fd&c Blue No. 1
- Fd&c Red No. 40
- Gelatin
- Hypromellose 2910 (6 Mpa.s)
- Ferric Oxide Yellow
- Isopropyl Alcohol
- Magnesium Carbonate
- Mannitol
- Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
- Polyethylene Glycol 6000
- Polysorbate 80
- Propylene Glycol
- Shellac
- Sodium Lauryl Sulfate
- Sodium Starch Glycolate Type a Corn
- Sucrose
- Talc
- Titanium Dioxide
Pharmaceutical Classes:
- Inhibition Gastric Acid Secretion [PE]
- 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.