Lansoprazole
- Product NDC
- 68016-758
- 11-digit product format
- 680160758
- Labeler code
- 68016
- Product ID
- 68016-758_e05d8f29-1055-4aef-ac88-f516e236303d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Chain Drug Consortium, LLC
- Application
- ANDA203187
- Marketing category
- ANDA
- Marketing start
- 2019-09-30
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- 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 |
|---|
| 68016-758-42 | 68016075842 | 3 BOTTLE, PLASTIC in 1 BOX (68016-758-42) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC | 2019-09-30 | 0000-00-00 | No | No | Current |