LINCO-SPECTIN 100 DIN 00813818
Status: Marketed
Holder: PHIBRO ANIMAL HEALTH CORPORATION
Molecule: LINCOMYCIN (LINCOMYCIN HYDROCHLORIDE)
Health Canada record
| Active ingredient(s) | LINCOMYCIN (LINCOMYCIN HYDROCHLORIDE) 33.3 G; SPECTINOMYCIN (SPECTINOMYCIN SULFATE) 66.7 G |
|---|---|
| Dosage form | Powder For Solution |
| Route | Oral |
| Schedule | PRESCRIPTION |
| Class | Veterinary |
| ATC | |
| Original market date | 31-Dec-1989 |
| Current status date | 09-Jul-2025 |
| Source | Health Canada DPD |
Establishment licence of the holder
Phibro Animal Health Ltd. — licence 3-002901, currently licensed, last inspection rating I (2026-06-23).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing LINCOMYCIN (LINCOMYCIN HYDROCHLORIDE)
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 00813893 | LINCO-SPECTIN | ZOETIS CANADA INC | Solution | LINCOMYCIN (LINCOMYCIN HYDROCHLORIDE) 50 MG; SPECTINOMYCIN (SPECTINOMYCIN SULFATE) 100 MG | Marketed |
| 00813761 | LINCOMIX | PHIBRO ANIMAL HEALTH CORPORATION | Powder For Solution | LINCOMYCIN (LINCOMYCIN HYDROCHLORIDE) 400 MG | Marketed |
| 00813745 | LINCOMIX 100 | ZOETIS CANADA INC | Solution | LINCOMYCIN (LINCOMYCIN HYDROCHLORIDE) 100 MG | Marketed |
| 00813648 | LINCOMIX 110 | PHIBRO ANIMAL HEALTH CORPORATION | Drug Premix | LINCOMYCIN (LINCOMYCIN HYDROCHLORIDE) 110 G | Marketed |
| 00813559 | LINCOMIX 44 | PHIBRO ANIMAL HEALTH CORPORATION | Drug Premix | LINCOMYCIN (LINCOMYCIN HYDROCHLORIDE) 44 G | Marketed |
| 02089882 | LINCOMYCIN 110 G | BIO AGRI MIX LP | Drug Premix | LINCOMYCIN (LINCOMYCIN HYDROCHLORIDE) 110 G | Marketed |
| 02091097 | LINCOMYCIN 44 G | BIO AGRI MIX LP | Drug Premix | LINCOMYCIN (LINCOMYCIN HYDROCHLORIDE) 44 G | Marketed |
| 02231271 | LINCOMYCIN SOLUBLE POWDER | BIO AGRI MIX LP | Powder | LINCOMYCIN (LINCOMYCIN HYDROCHLORIDE) 400 MG | Marketed |
| 02230947 | LINCOMYCIN SPECTINOMYCIN 100 SOLUBLE POWDER | BIO AGRI MIX LP | Powder For Solution | LINCOMYCIN (LINCOMYCIN HYDROCHLORIDE) 33.3 G; SPECTINOMYCIN (SPECTINOMYCIN HYDROCHLORIDE) 66.6 G | Marketed |
| 02209098 | LINCOMYCIN SPECTINOMYCIN 4.4% G PREMIX | BIO AGRI MIX LP | Drug Premix | LINCOMYCIN (LINCOMYCIN HYDROCHLORIDE) 22 G; SPECTINOMYCIN (SPECTINOMYCIN HYDROCHLORIDE) 22 G | Marketed |
| 00881430 | L-S 100 SOLUBLE POWDER | PFIZER CANADA INC ANIMAL HEALTH GROUP | Powder | LINCOMYCIN (LINCOMYCIN HYDROCHLORIDE) 33.3 G; SPECTINOMYCIN (SPECTINOMYCIN SULFATE) 66.7 G | Cancelled Post Market |
| 00813907 | L-S 20 | PHIBRO ANIMAL HEALTH CORPORATION | Drug Premix | LINCOMYCIN (LINCOMYCIN HYDROCHLORIDE) 22 G; SPECTINOMYCIN (SPECTINOMYCIN SULFATE) 22 G | Dormant |
| 00030732 | LINCOCIN | PFIZER CANADA ULC | Solution | LINCOMYCIN (LINCOMYCIN HYDROCHLORIDE) 300 MG | Cancelled Post Market |
| 00030589 | LINCOCIN | PFIZER CANADA ULC | Capsule | LINCOMYCIN (LINCOMYCIN HYDROCHLORIDE) 500 MG | Cancelled Post Market |
| 00813915 | LINCOCIN TABLETS 100MG | PHARMACIA ANIMAL HEALTH | Tablet | LINCOMYCIN (LINCOMYCIN HYDROCHLORIDE) 100 MG | Cancelled Post Market |
| 00813923 | LINCOCIN TABLETS 200MG | PHARMACIA ANIMAL HEALTH | Tablet | LINCOMYCIN (LINCOMYCIN HYDROCHLORIDE) 200 MG | Cancelled Post Market |
| 00813931 | LINCOCIN TABLETS 500MG | PHARMACIA ANIMAL HEALTH | Tablet | LINCOMYCIN (LINCOMYCIN HYDROCHLORIDE) 500 MG | Cancelled Post Market |
| 02424142 | LINCOMED 100 | BIMEDA-MTC ANIMAL HEALTH INC | Solution | LINCOMYCIN (LINCOMYCIN HYDROCHLORIDE) 100 MG | Dormant |
| 00813753 | LINCOMIX 8.8 PREMIX | PHARMACIA & UPJOHN ANIMAL HEALTH | Drug Premix | LINCOMYCIN (LINCOMYCIN HYDROCHLORIDE) 8.8 G | Cancelled Post Market |
| 02089874 | LINCOMYCIN 110 | BIO AGRI MIX LP | Drug Premix | LINCOMYCIN (LINCOMYCIN HYDROCHLORIDE) 110 G | Dormant |
| 02085844 | LINCOMYCIN 44 | BIO AGRI MIX LP | Drug Premix | LINCOMYCIN (LINCOMYCIN HYDROCHLORIDE) 44 G | Dormant |
| 02460718 | LINXMED-SP | BIMEDA-MTC ANIMAL HEALTH INC | Powder For Solution | LINCOMYCIN (LINCOMYCIN HYDROCHLORIDE) 400 MG | Dormant |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|---|---|---|
| 35634 | 2025-07-09 | New Drug Submission (NDS) | Administrative - Change in Product Ownership |
| 20272 | 2018-01-11 | Supplement to a New Drug Submission (SNDS) | CHANGE TO PRESCRIPTION STATUS. LABELLING UPDATES |
| 15179 | 2014-01-29 | New Drug Submission (NDS) | TRANSFER OF DRUG IDENTIFICATION NUMBER (DIN) HOLDER |
| 8643 | 2007-03-14 | New Drug Submission (NDS) | |
| 6150 | 2001-11-30 | New Drug Submission (NDS) | |
| 6724 | 1997-07-11 | New Drug Submission (NDS) |