PANTOPRAZOLE SODIUM
- Product NDC
- 60760-712
- 11-digit product format
- 607600712
- Labeler code
- 60760
- Product ID
- 60760-712_a6a8025b-d608-20ca-e053-2995a90a6f4d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PANTOPRAZOLE
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA202882
- Marketing category
- ANDA
- Marketing start
- 2020-03-04
- Marketing end
- 0000-00-00
- Substance
- PANTOPRAZOLE SODIUM
- Active strength
- 20 mg/1
- Pharmacologic classes
- Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60760-712 | PANTOPRAZOLE SODIUM (PANTOPRAZOLE) TABLET, DELAYED RELEASE [ST. MARY'S MEDICAL PARK PHARMACY] | 4 | Legacy NDC | 20241215_a0341042-1a55-73f6-e053-2a95a90a5b1b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-712-30 | 60760071230 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-712-30) | 2020-03-04 | 0000-00-00 | No | No | Current |
| 60760-712-60 | 60760071260 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-712-60) | 2020-03-04 | 0000-00-00 | No | No | Current |