basic care lansoprazole
- Product NDC
- 72288-829
- 11-digit product format
- 722880829
- Labeler code
- 72288
- Product ID
- 72288-829_ae98a412-94b4-4165-a794-3faa36d1ef67
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Amazon.com Services LLC
- Application
- NDA208025
- Marketing category
- NDA
- Marketing start
- 2021-08-09
- Substance
- LANSOPRAZOLE
- Active strength
- 15 mg/1
- Pharmacologic classes
- Inhibition Gastric Acid Secretion [PE], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 0K5C5T2QPG | LANSOPRAZOLE | 103577-45-3 | LANSOPRAZOLE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72288-829-55 | 72288082955 | 3 CARTON in 1 CARTON (72288-829-55) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK | 3 carton | 2021-08-09 | No | No | Historical |