lansoprazole
- Product NDC
- 60760-544
- 11-digit product format
- 607600544
- Labeler code
- 60760
- Product ID
- 60760-544_7ad086e3-91f9-fcb7-e053-2a91aa0acdfe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE PELLETS
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA202366
- Marketing category
- ANDA
- Marketing start
- 2018-03-14
- 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 |
|---|
| 60760-544-07 | 60760054407 | 7 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (60760-544-07) | 2018-03-14 | 0000-00-00 | No | No | Current |