penicillin v potassium

Generic: penicillin v potassium

Labeler: nucare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name penicillin v potassium
Generic Name penicillin v potassium
Labeler nucare pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

penicillin v potassium 250 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3176
Product ID 68071-3176_3892cc54-a21a-7666-e063-6294a90ae023
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065435
Listing Expiration 2026-12-31
Marketing Start 2008-04-29

Pharmacologic Class

Classes
penicillin-class antibacterial [epc] penicillins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713176
Hyphenated Format 68071-3176

Supplemental Identifiers

RxCUI
834061
UPC
0368071317640
UNII
146T0TU1JB

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 penicillin v potassium (source: ndc)
Generic Name penicillin v potassium (source: ndc)
Application Number ANDA065435 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE (68071-3176-2)
  • 30 TABLET, FILM COATED in 1 BOTTLE (68071-3176-3)
  • 40 TABLET, FILM COATED in 1 BOTTLE (68071-3176-4)
  • 6 TABLET, FILM COATED in 1 BOTTLE (68071-3176-6)
  • 28 TABLET, FILM COATED in 1 BOTTLE (68071-3176-8)
source: ndc

Packages (5)

68071-3176-2 20 TABLET, FILM COATED in 1 BOTTLE (68071-3176-2) 68071-3176-3 30 TABLET, FILM COATED in 1 BOTTLE (68071-3176-3) 68071-3176-4 40 TABLET, FILM COATED in 1 BOTTLE (68071-3176-4) 68071-3176-6 6 TABLET, FILM COATED in 1 BOTTLE (68071-3176-6) 68071-3176-8 28 TABLET, FILM COATED in 1 BOTTLE (68071-3176-8)

Ingredients (1)

penicillin v potassium (250 mg/1)

Linked Drug Pages (1)

Penicillin V Potassium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3892cc54-a21a-7666-e063-6294a90ae023", "openfda": {"upc": ["0368071317640"], "unii": ["146T0TU1JB"], "rxcui": ["834061"], "spl_set_id": ["4af2a165-0b7d-2539-e054-00144ff8d46c"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68071-3176-2)", "package_ndc": "68071-3176-2", "marketing_start_date": "20170317"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-3176-3)", "package_ndc": "68071-3176-3", "marketing_start_date": "20170317"}, {"sample": false, "description": "40 TABLET, FILM COATED in 1 BOTTLE (68071-3176-4)", "package_ndc": "68071-3176-4", "marketing_start_date": "20170317"}, {"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (68071-3176-6)", "package_ndc": "68071-3176-6", "marketing_start_date": "20170317"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (68071-3176-8)", "package_ndc": "68071-3176-8", "marketing_start_date": "20170317"}], "brand_name": "Penicillin V Potassium", "product_id": "68071-3176_3892cc54-a21a-7666-e063-6294a90ae023", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "68071-3176", "generic_name": "Penicillin V Potassium", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Penicillin V Potassium", "active_ingredients": [{"name": "PENICILLIN V POTASSIUM", "strength": "250 mg/1"}], "application_number": "ANDA065435", "marketing_category": "ANDA", "marketing_start_date": "20080429", "listing_expiration_date": "20261231"}