Lansoprazole
- Product NDC
- 11822-0019
- 11-digit product format
- 118220019
- Labeler code
- 11822
- Product ID
- 11822-0019_29bc0c52-cb89-c360-5d22-11c168b6b1ea
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Rite Aid Corporation
- Application
- ANDA202194
- Marketing category
- ANDA
- Marketing start
- 2022-10-01
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Lansoprazole
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LANSOPRAZOLE | 15 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0K5C5T2QPG |
| Rxcui | 596843 |
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11822-0019 | LANSOPRAZOLE CAPSULE, DELAYED RELEASE [RITE AID CORPORATION] | 4 | Current NDC, Legacy NDC | 20241203_9f424ff5-671b-ccaf-0682-929a27feb548.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-0019-1 | 11822001901 | 1 BOTTLE in 1 CARTON (11822-0019-1) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 1 bottle | 2022-10-01 | 0000-00-00 | No | No | Current |
| 11822-0019-3 | 11822001903 | 3 BOTTLE in 1 CARTON (11822-0019-3) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 3 bottle | 2022-10-01 | 0000-00-00 | No | No | Current |