NDC 0378-8030 – Lansoprazole
Lansoprazole 30 mg/1 · Capsule, Delayed Release Pellets · Oral
Product NDC0378-8030
Product details
- Brand name
- Lansoprazole
- Generic name
- lansoprazole
- Labeler
- Mylan Pharmaceuticals Inc.
- Dosage form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing category
- ANDA · ANDA090763
- Marketed since
- November 10, 2009
- Listing expires
- December 31, 2026
- Pharmacologic class
- Proton Pump Inhibitor
Active ingredients
- Lansoprazole 30 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 0378-8030-05 | 500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (0378-8030-05) | Nov 10, 2009 |
| 0378-8030-77 | 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (0378-8030-77) | Nov 10, 2009 |
| 0378-8030-93 | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (0378-8030-93) | Nov 10, 2009 |
Recalls mentioning this NDC
- D-147-2013 Feb 13, 2013 · Class II
Presence of Foreign Tablets/Capsules: Bottles of lansoprazole 30 mg delayed-release capsules may contain topiramate 100 mg tablets.
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