Details for New Drug Application (NDA): 080571
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NDA 080571 describes THIAMINE HYDROCHLORIDE, which is a drug marketed by Abraxis Pharm, Bel Mar, Caplin, Dell Labs, Dr Reddys, Epic Pharma Llc, Eugia Pharma, Fresenius Kabi Usa, Hospira, Luitpold, Mylan Institutional, Parke Davis, Sagent Pharms Inc, Watson Labs, West-ward Pharms Int, and Wyeth Ayerst, and is included in seventeen NDAs. It is available from thirteen suppliers. Additional details are available on the THIAMINE HYDROCHLORIDE profile page.
The generic ingredient in THIAMINE HYDROCHLORIDE is thiamine hydrochloride. There are seven drug master file entries for this compound. Thirteen suppliers are listed for this compound. Additional details are available on the thiamine hydrochloride profile page.
The generic ingredient in THIAMINE HYDROCHLORIDE is thiamine hydrochloride. There are seven drug master file entries for this compound. Thirteen suppliers are listed for this compound. Additional details are available on the thiamine hydrochloride profile page.
Summary for 080571
| Tradename: | THIAMINE HYDROCHLORIDE |
| Applicant: | Dr Reddys |
| Ingredient: | thiamine hydrochloride |
| Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 080571
Suppliers and Packaging for NDA: 080571
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| THIAMINE HYDROCHLORIDE | thiamine hydrochloride | INJECTABLE;INJECTION | 080571 | ANDA | Henry Schein, Inc. | 0404-9799 | 0404-9799-20 | 1 VIAL, MULTI-DOSE in 1 BAG (0404-9799-20) / 2 mL in 1 VIAL, MULTI-DOSE |
| THIAMINE HYDROCHLORIDE | thiamine hydrochloride | INJECTABLE;INJECTION | 080571 | ANDA | Dr. Reddy's Laboratories Inc. | 43598-050 | 43598-050-25 | 25 VIAL, MULTI-DOSE in 1 CARTON (43598-050-25) / 2 mL in 1 VIAL, MULTI-DOSE (43598-050-11) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 100MG/ML | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | AP | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 200MG/ML | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | RLD: | No | |||||
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