Over-the-counter drug · ANDA
Omeprazole and sodium bicarbonate (Omeprazole, sodium bicarbonate) NDC 37808-732
Omeprazole 20 mg/1; Sodium bicarbonate 1100 mg/1 · Capsule, Gelatin coated · Oral · H E B
NDC codes
FDA NDC DirectoryProduct NDC (as listed)37808-732Labeler and product segments. Claims need a package NDC.
Product NDC at billing width37808-0732Add the package segment from the table below.
| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 37808-732-01 | 3780807320137808073201 | 1 BOTTLE in 1 CARTON (37808-732-01) / 14 CAPSULE, GELATIN COATED in 1 BOTTLEMarketed from Aug 25, 2017 | |
| 37808-732-03 | 3780807320337808073203 | 3 BOTTLE in 1 CARTON (37808-732-03) / 14 CAPSULE, GELATIN COATED in 1 BOTTLEMarketed from Aug 25, 2017 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Omeprazole and sodium bicarbonate
- Generic name (nonproprietary)
- omeprazole, sodium bicarbonate
- Active ingredients
- Omeprazole — 20 mg/1Sodium bicarbonate — 1100 mg/1
- Dosage form
- Capsule, Gelatin coated
- Route
- Oral
- Labeler
- H E BNDC labeler code 37808
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 201361
- Marketing start
- Listing expires
- Other FDA classes
- Cytochrome P450 2C19 Inhibitors (Mechanism)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Proton Pump Inhibitors (Mechanism)
- Identifiers
- Product ID 37808-732_99b31e8b-1cf3-47a5-b0f7-31e0530691edSPL ID 99b31e8b-1cf3-47a5-b0f7-31e0530691edSPL set ID ddc8d73f-f4a1-42a7-89ee-420346820f61RxCUI 616539UNII KG60484QX9, 8MDF5V39QO
- Pharmacologic class
- Osmotic Laxative; Proton Pump Inhibitor
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N437808073201followed by a unit qualifier and the quantityPackage 37808-0732-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Use • treats frequent heartburn (occurs 2 or more days a week) • not intended for immediate relief of heartburn. This drug may take 1 to 4 days for full effect.
Excerpt only. Read the full label for complete information.
About NDC 37808-732
- What is NDC 37808-732?
- 37808-732 is the product NDC for Omeprazole and sodium bicarbonate, Omeprazole 20 mg/1; Sodium bicarbonate 1100 mg/1 capsule, gelatin coated, listed with the FDA by H E B. It has 2 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Omeprazole and sodium bicarbonate (Omeprazole, sodium bicarbonate).
- What is the active ingredient?
- Omeprazole, Sodium bicarbonate.
- Who is the labeler?
- H E B, NDC labeler code 37808. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Omeprazole and sodium bicarbonate?
- 19 other product NDCs are listed under this name. See all Omeprazole and sodium bicarbonate NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Omeprazole and sodium bicarbonate products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Omeprazole And Sodium Bicarbonate | Omeprazole 20 mg/1; Sodium bicarbonate 1100 mg/1 | CapsuleOral | Aurohealth LLC | 58602-732 | 58602-0732-0558602-0732-5758602-0732-60 |
| omeprazole and sodium bicarbonateomeprazole, sodium bicarbonate | Omeprazole 20 mg/1; Sodium bicarbonate 1100 mg/1 | Capsule, Gelatin coatedOral | Amazon.com Services LLC | 72288-564 | 72288-0564-03 |
| Omeprazole and Sodium Bicarbonate | Omeprazole 20 mg/1; Sodium bicarbonate 1680 mg/1 | Powder, For suspensionOral | ANI Pharmaceuticals, Inc. | 70954-797 | 70954-0797-20 |
| Omeprazole and Sodium Bicarbonate | Omeprazole 40 mg/1; Sodium bicarbonate 1680 mg/1 | Powder, For suspensionOral | ANI Pharmaceuticals, Inc. | 70954-798 | 70954-0798-20 |
| Omeprazole and Sodium Bicarbonate | Omeprazole 40 mg/1; Sodium bicarbonate 1100 mg/1 | CapsuleOral | PHOENIX RX LLC | 85509-1032 | 85509-1032-0185509-1032-0385509-1032-06 |
| Omeprazole and Sodium Bicarbonate | Omeprazole 20 mg/1; Sodium bicarbonate 1680 mg/1 | Powder, For suspensionOral | Dr. Reddy's Laboratories Inc., | 43598-010 | 43598-0010-0143598-0010-1443598-0010-28+1 more |
| Omeprazole and Sodium Bicarbonate | Omeprazole 20 mg/1; Sodium bicarbonate 1680 mg/1 | Powder, For suspensionOral | Dr. Reddy's Laboratories Inc., | 43598-307 | 43598-0307-0143598-0307-1443598-0307-28+1 more |
| Omeprazole and Sodium Bicarbonate | Omeprazole 20 mg/1; Sodium bicarbonate 1680 mg/1 | Powder, For suspensionOral | Dr. Reddy's Laboratories Inc., | 75907-138 | 75907-0138-42 |
| Omeprazole And Sodium Bicarbonate | Omeprazole 20 mg/1; Sodium bicarbonate 1100 mg/1 | CapsuleOral | Aurohealth LLC | 58602-725 | 58602-0725-0558602-0725-5758602-0725-60 |
| omeprazole and sodium bicarbonateomeprazole, sodium bicarbonate | Omeprazole 20 mg/1; Sodium bicarbonate 1100 mg/1 | Capsule, Gelatin coatedOral | Meijer Distribution Inc | 41250-938 | 41250-0938-03 |
Other NDCs under ANDA 201361
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| basic care omeprazole and sodium bicarbonateomeprazole, sodium bicarbonate | Omeprazole 20 mg/1; Sodium bicarbonate 1100 mg/1 | Capsule, Gelatin coatedOral | Amazon.com Services LLC | 72288-732 |
| Good Sense Omeprazole and Sodium Bicarbonateomeprazole, sodium bicarbonate | Omeprazole 20 mg/1; Sodium bicarbonate 1100 mg/1 | Capsule, Gelatin coatedOral | L. Perrigo Company | 0113-0058 |
| omeprazole and sodium bicarbonateomeprazole, sodium bicarbonate | Omeprazole 20 mg/1; Sodium bicarbonate 1100 mg/1 | Capsule, Gelatin coatedOral | Meijer Distribution Inc | 41250-938 |
| Zegerid OTComepraole, sodium bicarbonate | Omeprazole 20 mg/1; Sodium bicarbonate 1100 mg/1 | Capsule, Gelatin coatedOral | Riley Consumer Care LLC | 82632-699 |
| omeprazole and sodium bicarbonateomeprazole, sodium bicarbonate | Omeprazole 20 mg/1; Sodium bicarbonate 1100 mg/1 | Capsule, Gelatin coatedOral | Amazon.com Services LLC | 72288-564 |
| Omeprazole and sodium bicarbonateomeprazole, sodium bicarbonate | Omeprazole 20 mg/1; Sodium bicarbonate 1100 mg/1 | Capsule, Gelatin coatedOral | Walgreen Company | 0363-0732 |
| equate omeprazole and sodium bicarbonateomeprazole, sodium bicarbonate | Omeprazole 20 mg/1; Sodium bicarbonate 1100 mg/1 | Capsule, Gelatin coatedOral | WALMART INC. | 79903-013 |
| Omeprazole and Sodium Bicarbonateomeprazole, sodium bicarbonate | Omeprazole 20 mg/1; Sodium bicarbonate 1100 mg/1 | Capsule, Gelatin coatedOral | CVS Pharmacy | 59779-732 |