Details for New Drug Application (NDA): 018558
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NDA 018558 describes LITHIUM CARBONATE, which is a drug marketed by Able, Alembic Ltd, Apotex Inc, Glenmark Pharms Ltd, Hetero Labs Ltd Iii, Hikma, Norvium Bioscience, Usl Pharma, Watson Labs, Alembic, Glenmark Pharms Inc, Heritage Pharma, Hikma Intl Pharms, Mylan Pharms Inc, Unique, Pfizer, and Sun Pharm Inds Inc, and is included in twenty-nine NDAs. It is available from twenty-three suppliers. Additional details are available on the LITHIUM CARBONATE profile page.
The generic ingredient in LITHIUM CARBONATE is lithium carbonate. There are fifteen drug master file entries for this compound. Twenty-four suppliers are listed for this compound. Additional details are available on the lithium carbonate profile page.
The generic ingredient in LITHIUM CARBONATE is lithium carbonate. There are fifteen drug master file entries for this compound. Twenty-four suppliers are listed for this compound. Additional details are available on the lithium carbonate profile page.
Summary for 018558
| Tradename: | LITHIUM CARBONATE |
| Applicant: | Hikma |
| Ingredient: | lithium carbonate |
| Patents: | 0 |
Suppliers and Packaging for NDA: 018558
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| LITHIUM CARBONATE | lithium carbonate | TABLET;ORAL | 018558 | NDA | Hikma Pharmaceuticals USA Inc. | 0054-4527 | 0054-4527-25 | 100 TABLET in 1 BOTTLE (0054-4527-25) |
| LITHIUM CARBONATE | lithium carbonate | TABLET;ORAL | 018558 | NDA | Hikma Pharmaceuticals USA Inc. | 0054-4527 | 0054-4527-31 | 1000 TABLET in 1 BOTTLE (0054-4527-31) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 300MG | ||||
| Approval Date: | Jan 29, 1982 | TE: | AB | RLD: | Yes | ||||
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