lincomycin

Generic: lincomycin hydrochloride

Labeler: pai holdings, llc dba pai pharma
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lincomycin
Generic Name lincomycin hydrochloride
Labeler pai holdings, llc dba pai pharma
Dosage Form INJECTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

lincomycin hydrochloride 3000 mg/10mL

Manufacturer
PAI Holdings, LLC dba PAI Pharma

Identifiers & Regulatory

Product NDC 0121-1035
Product ID 0121-1035_23f95ea6-ad32-a143-e063-6394a90ae77c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212770
Listing Expiration 2026-12-31
Marketing Start 2024-10-07

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01211035
Hyphenated Format 0121-1035

Supplemental Identifiers

RxCUI
239212
UNII
M6T05Z2B68

Packaging Origin

Original Packager
true

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 lincomycin (source: ndc)
Generic Name lincomycin hydrochloride (source: ndc)
Application Number ANDA212770 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 3000 mg/10mL
source: ndc
Packaging
  • 10 VIAL, MULTI-DOSE in 1 CARTON (0121-1035-55) / 10 mL in 1 VIAL, MULTI-DOSE
source: ndc

Packages (1)

Ingredients (1)

lincomycin hydrochloride (3000 mg/10mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "23f95ea6-ad32-a143-e063-6394a90ae77c", "openfda": {"unii": ["M6T05Z2B68"], "rxcui": ["239212"], "spl_set_id": ["23f9608c-3126-35db-e063-6294a90af054"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 CARTON (0121-1035-55)  / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "0121-1035-55", "marketing_start_date": "20241007"}], "brand_name": "Lincomycin", "product_id": "0121-1035_23f95ea6-ad32-a143-e063-6394a90ae77c", "dosage_form": "INJECTION", "product_ndc": "0121-1035", "generic_name": "Lincomycin Hydrochloride", "labeler_name": "PAI Holdings, LLC dba PAI Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lincomycin", "active_ingredients": [{"name": "LINCOMYCIN HYDROCHLORIDE", "strength": "3000 mg/10mL"}], "application_number": "ANDA212770", "marketing_category": "ANDA", "marketing_start_date": "20241007", "listing_expiration_date": "20261231"}