Lansoprazole
- Product NDC
- 68071-1972
- 11-digit product format
- 680711972
- Labeler code
- 68071
- Product ID
- 68071-1972_49123659-5488-0fb5-e054-00144ff8d46c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 68071-1972-3 | 2020-07-10 | C162847 | 48780-1 | 9d75b9d0-2875-f424-e053-dadaa90a57ce | 49123659-5487-0fb5-e054-00144ff8d46c |
| 68071-1972-6 | 2020-07-10 | C162847 | 48780-1 | 9d75b9d0-2875-f424-e053-dadaa90a57ce | 49123659-5487-0fb5-e054-00144ff8d46c |
| 68071-1972-7 | 2020-07-10 | C162847 | 48780-1 | 9d75b9d0-2875-f424-e053-dadaa90a57ce | 49123659-5487-0fb5-e054-00144ff8d46c |
| 68071-1972-3 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-2875-f424-e053-dadaa90a57ce | 49123659-5487-0fb5-e054-00144ff8d46c |
| 68071-1972-6 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-2875-f424-e053-dadaa90a57ce | 49123659-5487-0fb5-e054-00144ff8d46c |
| 68071-1972-7 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-2875-f424-e053-dadaa90a57ce | 49123659-5487-0fb5-e054-00144ff8d46c |