Carboxymethylcellulose sodium
- Product NDC
- 49668-001
- 11-digit product format
- 496680001
- Labeler code
- 49668
- Product ID
- 49668-001_3aba460a-1912-4794-a317-f477af962b40
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Carboxymethylcellulose sodium
- Dosage form
- SOLUTION
- Route
- OPHTHALMIC
- Labeler
- PROMED EXPORTS PRIVATE LIMITED
- Application
- part349
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2009-10-01
- Marketing end
- 0000-00-00
- Substance
- CARBOXYMETHYLCELLULOSE SODIUM
- Active strength
- 5 mg/mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 49668-001-01 | Carboxymethylcellulose sodium | 0.4 mL in 1 VIAL, SINGLE-DOSE | SOLUTION | 0.4 | | 1 |
| 49668-001-01 | Carboxymethylcellulose sodium | 30 in 1 CONTAINER | SOLUTION | 30 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49668-001 | CARBOXYMETHYLCELLULOSE SODIUM SOLUTION [PROMED EXPORTS PRIVATE LIMITED] | 1 | Legacy NDC, 2 package rows | 20091001_3aba460a-1912-4794-a317-f477af962b40.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 49668-001-01 | 49668000101 | 0.4 mL in 1 VIAL, SINGLE-DOSE | 0.4 ml | Historical |