ampicillin
Generic: ampicillin
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
ampicillin
Generic Name
ampicillin
Labeler
remedyrepack inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
ampicillin trihydrate 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-2607
Product ID
70518-2607_4a799860-01be-631a-e063-6294a90aea08
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA064082
Listing Expiration
2027-12-31
Marketing Start
2020-02-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705182607
Hyphenated Format
70518-2607
Supplemental Identifiers
RxCUI
UNII
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
ampicillin (source: ndc)
Generic Name
ampicillin (source: ndc)
Application Number
ANDA064082 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 28 CAPSULE in 1 BOTTLE, PLASTIC (70518-2607-0)
- 28 CAPSULE in 1 BOTTLE, PLASTIC (70518-2607-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4a799860-01be-631a-e063-6294a90aea08", "openfda": {"unii": ["HXQ6A1N7R6"], "rxcui": ["308212"], "spl_set_id": ["4134cd79-c895-4e6e-b1d5-8e01c38bf2d1"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "28 CAPSULE in 1 BOTTLE, PLASTIC (70518-2607-0)", "package_ndc": "70518-2607-0", "marketing_start_date": "20200228"}, {"sample": false, "description": "28 CAPSULE in 1 BOTTLE, PLASTIC (70518-2607-1)", "package_ndc": "70518-2607-1", "marketing_start_date": "20250717"}], "brand_name": "Ampicillin", "product_id": "70518-2607_4a799860-01be-631a-e063-6294a90aea08", "dosage_form": "CAPSULE", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "70518-2607", "generic_name": "Ampicillin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ampicillin", "active_ingredients": [{"name": "AMPICILLIN TRIHYDRATE", "strength": "500 mg/1"}], "application_number": "ANDA064082", "marketing_category": "ANDA", "marketing_start_date": "20200228", "listing_expiration_date": "20271231"}