Dorzolamide PF
- Product NDC
- 70261-516
- 11-digit product format
- 702610516
- Labeler code
- 70261
- Product ID
- 70261-516_6bb681e9-0fc8-7e5c-e053-2991aa0a7c65
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dorzolamide PF
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- ImprimisRx NJ
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2018-01-01
- Marketing end
- 0000-00-00
- Substance
- DORZOLAMIDE HYDROCHLORIDE
- Active strength
- 20 mg/mL
- Pharmacologic classes
- Carbonic Anhydrase Inhibitor [EPC],Carbonic Anhydrase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 70261-516-10 | Dorzolamide PF | 10 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 10 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70261-516 | DORZOLAMIDE PF SOLUTION/ DROPS [IMPRIMISRX NJ] | 1 | Legacy NDC, 1 package rows | 20180508_6bb681e9-0fc7-7e5c-e053-2991aa0a7c65.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 70261-516-10 | 70261051610 | 10 mL in 1 BOTTLE, DROPPER | 10 ml | Historical |