Lansoprazole
- Product NDC
- 70700-262
- 11-digit product format
- 707000262
- Labeler code
- 70700
- Product ID
- 70700-262_ce9167b4-3b92-9cbd-f4f5-a8788ed0d47a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Xiromed LLC
- Application
- ANDA203203
- Marketing category
- ANDA
- Marketing start
- 2018-08-24
- 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 | 311277, 596843 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70700-262-30 | Lansoprazole | 30 in 1 BOTTLE | CAPSULE, DELAYED RELEASE | 30 | | 22 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70700-262 | LANSOPRAZOLE CAPSULE, DELAYED RELEASE [XIROMED LLC] | 22 | Current NDC, Legacy NDC, 1 package rows | 20230707_00a574e0-bd03-deea-9f85-b108f78982ba.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70700-262-30 | 70700026230 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70700-262-30) | 2018-08-24 | 0000-00-00 | No | No | Current |