Lansoprazole
- Product NDC
- 0363-0037
- 11-digit product format
- 003630037
- Labeler code
- 0363
- Product ID
- 0363-0037_9e2ef05d-952e-deac-7e2d-dc6db9b2ee57
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Walgreens company
- Application
- ANDA202194
- Marketing category
- ANDA
- Marketing start
- 2023-01-15
- 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 |
|---|
| 0363-0037 | LANSOPRAZOLE CAPSULE, DELAYED RELEASE [WALGREENS COMPANY] | 3 | Current NDC | 20241203_277093d5-cd0f-36ad-63d4-824a62d2a16c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0363-0037-14 | 00363003714 | 1 BOTTLE in 1 CARTON (0363-0037-14) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 1 bottle | 2023-01-15 | No | No | Current |
| 0363-0037-28 | 00363003728 | 2 BOTTLE in 1 CARTON (0363-0037-28) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 2 bottle | 2023-01-15 | No | No | Current |
| 0363-0037-42 | 00363003742 | 3 BOTTLE in 1 CARTON (0363-0037-42) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 3 bottle | 2023-01-15 | No | No | Current |