Lansoprazole
- Product NDC
- 72162-1976
- 11-digit product format
- 721621976
- Labeler code
- 72162
- Product ID
- 72162-1976_c1322bac-7271-4549-af07-9edf03f204c3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203203
- Marketing category
- ANDA
- Marketing start
- 2018-08-24
- Substance
- LANSOPRAZOLE
- Active strength
- 30 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1976-3 | 72162197603 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72162-1976-3) | 2024-02-06 | No | No | Historical |
| 72162-1976-5 | 72162197605 | 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72162-1976-5) | 2024-02-06 | No | No | Historical |
| 72162-1976-9 | 72162197609 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72162-1976-9) | 2024-02-06 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Lansoprazole | Bryant Ranch Prepack | 2024-02-06 | HUMAN PRESCRIPTION DRUG LABEL | 100 |