Not Applicable
- Product NDC
- 69336-112
- 11-digit product format
- 693360112
- Labeler code
- 69336
- Product ID
- 69336-112_871465bc-55d1-4b4e-97d9-8591d705d78c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- omeprazole sodium bicarbonate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Sterling Knight Pharmaceuticals LLC
- Application
- ANDA207476
- Marketing category
- ANDA
- Marketing start
- 2017-07-13
- Marketing end
- 0000-00-00
- Substance
- OMEPRAZOLE; SODIUM BICARBONATE
- Active strength
- 40 mg/1; mg/1
- Pharmacologic classes
- Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69336-112-30 | Not Applicable | 30 in 1 PACKAGE | CAPSULE | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69336-112 | NOT APPLICABLE (OMEPRAZOLE SODIUM BICARBONATE) CAPSULE [STERLING KNIGHT PHARMACEUTICALS LLC] | 1 | Legacy NDC, 1 package rows | 20170714_f77428fd-1744-4b3f-bd9c-b7fde46a211a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 69336-112-30 | 69336011230 | 30 in 1 PACKAGE | Historical |