ampicillin
Generic: ampicillin
Labeler: sandoz incDrug Facts
Product Profile
Brand Name
ampicillin
Generic Name
ampicillin
Labeler
sandoz inc
Dosage Form
CAPSULE
Routes
Active Ingredients
ampicillin trihydrate 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0781-2145
Product ID
0781-2145_0202d39a-7586-4abd-9b9f-ac935aadccf2
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA064082
Listing Expiration
2026-12-31
Marketing Start
1995-08-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
07812145
Hyphenated Format
0781-2145
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
- 100 CAPSULE in 1 BOTTLE (0781-2145-01)
- 500 CAPSULE in 1 BOTTLE (0781-2145-05)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0202d39a-7586-4abd-9b9f-ac935aadccf2", "openfda": {"upc": ["0307812145050", "0307812145012"], "unii": ["HXQ6A1N7R6"], "rxcui": ["308212", "313800"], "spl_set_id": ["0a66c5c3-63bf-46e3-835e-26b555ab6954"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0781-2145-01)", "package_ndc": "0781-2145-01", "marketing_start_date": "19950829"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (0781-2145-05)", "package_ndc": "0781-2145-05", "marketing_start_date": "19950829"}], "brand_name": "Ampicillin", "product_id": "0781-2145_0202d39a-7586-4abd-9b9f-ac935aadccf2", "dosage_form": "CAPSULE", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "0781-2145", "generic_name": "Ampicillin", "labeler_name": "Sandoz 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": "19950829", "listing_expiration_date": "20261231"}