Lansoprazole
- Product NDC
- 63739-555
- 11-digit product format
- 637390555
- Labeler code
- 63739
- Product ID
- 63739-555_bd0ae02e-f5f4-1aaf-e053-2a95a90adda2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA091269
- Marketing category
- ANDA
- Marketing start
- 2010-10-15
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63739-555-10 | 63739055510 | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-555-10) > 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK | 10 blister pack | 2010-10-15 | 0000-00-00 | No | No | Current |
| 63739-555-41 | 63739055541 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, UNIT-DOSE (63739-555-41) | | 2019-05-08 | 2021-04-30 | No | No | Current |