Lansoprazole
- Product NDC
- 37808-755
- 11-digit product format
- 378080755
- Labeler code
- 37808
- Product ID
- 37808-755_0427e266-6d64-4f89-8e1a-dae50a33c3be
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- H E B
- Application
- ANDA203187
- Marketing category
- ANDA
- Marketing start
- 2019-09-30
- Marketing end
- 0000-00-00
- Substance
- LANSOPRAZOLE
- Active strength
- 15 mg/1
- Pharmacologic classes
- Inhibition Gastric Acid Secretion [PE], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 37808-755 | LANSOPRAZOLE CAPSULE, DELAYED RELEASE [H E B] | 6 | Legacy NDC | 20250306_3f13e813-1283-45a5-8fc3-0dc44009c82b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37808-755-14 | 37808075514 | 1 BOTTLE, PLASTIC in 1 BOX (37808-755-14) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC | 2019-09-30 | 0000-00-00 | No | No | Current |
| 37808-755-42 | 37808075542 | 3 BOTTLE, PLASTIC in 1 BOX (37808-755-42) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC | 2019-09-30 | 0000-00-00 | No | No | Current |