Lansoprazole
- Product NDC
- 55700-814
- 11-digit product format
- 557000814
- Labeler code
- 55700
- Product ID
- 55700-814_6802f5dd-b7b8-4791-bd38-a3332fdfbe61
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE PELLETS
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA207156
- Marketing category
- ANDA
- Marketing start
- 2019-11-08
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-814-30 | 55700081430 | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (55700-814-30) | 2019-11-08 | 0000-00-00 | No | No | Current |