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Thiamine Hydrochloride
Thiamine Hydrochloride - 67457-196-02 - (thiamine hydrochloride)
Drug Information of Thiamine Hydrochloride
| Product NDC: | 67457-196 |
| Proprietary Name: | Thiamine Hydrochloride |
| Non Proprietary Name: | thiamine hydrochloride |
| Active Ingredient(s): | 100 mg/mL & nbsp; thiamine hydrochloride |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Thiamine Hydrochloride
| Product NDC: | 67457-196 |
| Labeler Name: | Mylan Institutional LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091623 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130604 |
Package Information of Thiamine Hydrochloride
| Package NDC: | 67457-196-02 |
| Package Description: | 25 VIAL, MULTI-DOSE in 1 CARTON (67457-196-02) > 2 mL in 1 VIAL, MULTI-DOSE (67457-196-00) |
NDC Information of Thiamine Hydrochloride
| NDC Code | 67457-196-02 |
| Proprietary Name | Thiamine Hydrochloride |
| Package Description | 25 VIAL, MULTI-DOSE in 1 CARTON (67457-196-02) > 2 mL in 1 VIAL, MULTI-DOSE (67457-196-00) |
| Product NDC | 67457-196 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | thiamine hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20130604 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Institutional LLC |
| Substance Name | THIAMINE HYDROCHLORIDE |
| Strength Number | 100 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
