LANSOPRAZOLE
- Product NDC
- 69336-107
- 11-digit product format
- 693360107
- Labeler code
- 69336
- Product ID
- 69336-107_941762b8-d5ca-412c-99d4-e56dc9e2cd7b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LANSOPRAZOLE
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Sterling Knight Pharmaceuticals LLC
- Application
- ANDA201921
- Marketing category
- ANDA
- Marketing start
- 2016-10-31
- Marketing end
- 0000-00-00
- Substance
- LANSOPRAZOLE
- Active strength
- 30 mg/1
- Pharmacologic classes
- Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Inhibition Gastric Acid Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69336-107-30 | LANSOPRAZOLE | 30 in 1 BOTTLE | CAPSULE, DELAYED RELEASE | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69336-107 | LANSOPRAZOLE CAPSULE, DELAYED RELEASE [STERLING KNIGHT PHARMACEUTICALS LLC] | 1 | Legacy NDC, 1 package rows | 20161031_1cf560fe-df28-44df-8e33-30409f33f2ef.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 69336-107-30 | 69336010730 | 30 in 1 BOTTLE | Historical |