omeprazole/bicarbonate
Generic: omeprazole and sodium bicarbonate
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
omeprazole/bicarbonate
Generic Name
omeprazole and sodium bicarbonate
Labeler
proficient rx lp
Dosage Form
CAPSULE, GELATIN COATED
Routes
Active Ingredients
omeprazole 40 mg/1, sodium bicarbonate 1100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71205-985
Product ID
71205-985_f35ea0c8-7b13-4fe6-9b43-2bbcb916250d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207476
Listing Expiration
2026-12-31
Marketing Start
2018-07-27
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71205985
Hyphenated Format
71205-985
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
omeprazole/bicarbonate (source: ndc)
Generic Name
omeprazole and sodium bicarbonate (source: ndc)
Application Number
ANDA207476 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/1
- 1100 mg/1
Packaging
- 30 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (71205-985-30)
- 60 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (71205-985-60)
- 90 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (71205-985-90)
Packages (3)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f35ea0c8-7b13-4fe6-9b43-2bbcb916250d", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000182140"], "upc": ["0371205984601", "0371205985608"], "unii": ["KG60484QX9", "8MDF5V39QO"], "rxcui": ["616539", "616541"], "spl_set_id": ["4d642036-7175-4f29-9f07-dbd282231d4a"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (71205-985-30)", "package_ndc": "71205-985-30", "marketing_start_date": "20200501"}, {"sample": false, "description": "60 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (71205-985-60)", "package_ndc": "71205-985-60", "marketing_start_date": "20200501"}, {"sample": false, "description": "90 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (71205-985-90)", "package_ndc": "71205-985-90", "marketing_start_date": "20200501"}], "brand_name": "Omeprazole/Bicarbonate", "product_id": "71205-985_f35ea0c8-7b13-4fe6-9b43-2bbcb916250d", "dosage_form": "CAPSULE, GELATIN COATED", "pharm_class": ["Alkalinizing Activity [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "71205-985", "generic_name": "Omeprazole and Sodium Bicarbonate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Omeprazole/Bicarbonate", "active_ingredients": [{"name": "OMEPRAZOLE", "strength": "40 mg/1"}, {"name": "SODIUM BICARBONATE", "strength": "1100 mg/1"}], "application_number": "ANDA207476", "marketing_category": "ANDA", "marketing_start_date": "20180727", "listing_expiration_date": "20261231"}