LANSOPRAZOLE
- Product NDC
- 51991-772
- 11-digit product format
- 519910772
- Labeler code
- 51991
- Product ID
- 51991-772_a2884a15-5249-4f2e-ae9f-bbf2f942421e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LANSOPRAZOLE
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Breckenridge Pharmaceutical, Inc.
- Application
- ANDA201921
- Marketing category
- ANDA
- Marketing start
- 2012-12-18
- Marketing end
- 2021-05-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51991-772-01 | 51991077201 | 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (51991-772-01) | 2012-12-18 | 2021-05-31 | No | No | Current |
| 51991-772-05 | 51991077205 | 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (51991-772-05) | 2012-12-18 | 2021-04-30 | No | No | Current |
| 51991-772-10 | 51991077210 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (51991-772-10) | 2012-12-18 | 2021-05-31 | No | No | Current |
| 51991-772-33 | 51991077233 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (51991-772-33) | 2012-12-18 | 2021-05-31 | No | No | Current |
| 51991-772-90 | 51991077290 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (51991-772-90) | 2012-12-18 | 2021-05-31 | No | No | Current |