ALOMIDE
- Product NDC
- 0078-0736
- 11-digit product format
- 000780736
- Labeler code
- 0078
- Product ID
- 0078-0736_74317375-53a5-44f7-91ea-aa5f5cfe1851
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lodoxamide tromethamine
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Novartis Pharmaceuticals Corporation
- Application
- NDA020191
- Marketing category
- NDA
- Marketing start
- 1993-09-30
- Marketing end
- 0000-00-00
- Substance
- LODOXAMIDE TROMETHAMINE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Decreased Histamine Release [PE], Mast Cell Stabilizer [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0078-0736-10 | 00078073610 | 1 BOTTLE in 1 CARTON (0078-0736-10) > 10 mL in 1 BOTTLE | 1 bottle | 2022-08-15 | 0000-00-00 | No | No | Current |