erythromycin
- Product NDC
- 71205-265
- 11-digit product format
- 712050265
- Labeler code
- 71205
- Product ID
- 71205-265_e81dd1b8-6a0c-4fc4-afbe-496ed719c048
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- erythromycin
- Dosage form
- OINTMENT
- Route
- OPHTHALMIC
- Labeler
- Proficient Rx LP
- Application
- ANDA062447
- Marketing category
- ANDA
- Marketing start
- 2014-05-08
- Marketing end
- 0000-00-00
- Substance
- ERYTHROMYCIN
- Active strength
- 5 mg/g
- Pharmacologic classes
- Decreased Sebaceous Gland Activity [PE], Macrolide Antimicrobial [EPC], Macrolide [EPC], Macrolides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-265 | ERYTHROMYCIN OINTMENT [PROFICIENT RX LP] | 4 | Legacy NDC | 20220710_d0dd105b-1ad4-4dd9-ba26-4fc889050009.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-265-35 | 71205026535 | 1 TUBE in 1 CARTON (71205-265-35) > 3.5 g in 1 TUBE | 1 tube | 2019-05-01 | 0000-00-00 | No | No | Current |