Pantoprazole Sodium
- Product NDC
- 70518-0395
- 11-digit product format
- 705180395
- Labeler code
- 70518
- Product ID
- 70518-0395_8469dbff-b65f-70d0-e053-2991aa0af684
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077056
- Marketing category
- ANDA
- Marketing start
- 2017-04-04
- Marketing end
- 0000-00-00
- Substance
- PANTOPRAZOLE SODIUM
- Active strength
- 40 mg/1
- Pharmacologic classes
- Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record