carboxymethylcellulose sodium
- Product NDC
- 50268-065
- 11-digit product format
- 502680065
- Labeler code
- 50268
- Product ID
- 50268-065_47e225fb-3d2e-4f80-e063-6394a90aff85
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- carboxymethylcellulose sodium
- Dosage form
- GEL
- Route
- OPHTHALMIC
- Labeler
- AvPAK
- Application
- M018
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-11-18
- Substance
- CARBOXYMETHYLCELLULOSE SODIUM
- Active strength
- 10 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- carboxymethylcellulose sodium
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CARBOXYMETHYLCELLULOSE SODIUM | 10 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | K679OBS311 |
| Rxcui | 579907 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50268-065-30 | carboxymethylcellulose sodium | 0.4 mL in 1 VIAL, SINGLE-USE | GEL | 0.4 | | 6 |
| 50268-065-30 | carboxymethylcellulose sodium | 30 in 1 CARTON | GEL | 30 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50268-065 | CARBOXYMETHYLCELLULOSE SODIUM GEL [AVPAK] | 5 | Current NDC, Legacy NDC, 2 package rows | 20240308_b4697319-438e-2ec8-e053-2a95a90abb56.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50268-065-30 | 50268006530 | 30 VIAL, SINGLE-USE in 1 CARTON (50268-065-30) / .4 mL in 1 VIAL, SINGLE-USE | 2020-11-18 | 0000-00-00 | No | No | Current |