Dyabetex
- Product NDC
- 43074-108
- 11-digit product format
- 430740108
- Labeler code
- 43074
- Product ID
- 43074-108_683dc33c-ba75-4a12-acb1-e82d0ea98d78
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TETRACYCLINE HYDROCHLORIDE
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Phillips Company
- Application
- part333B
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2010-08-24
- Marketing end
- 0000-00-00
- Substance
- TETRACYCLINE HYDROCHLORIDE
- Active strength
- 0 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 |
|---|
| 43074-108-01 | Dyabetex | 3 mL in 1 BOTTLE, DROPPER | OINTMENT | 3 | | 1 |
| 43074-108-02 | Dyabetex | 1 in 1 BOTTLE, PLASTIC | OINTMENT | 1 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43074-108 | DYABETEX (TETRACYCLINE HYDROCHLORIDE) OINTMENT [PHILLIPS COMPANY] | 1 | Legacy NDC, 2 package rows | 20100907_2c2b4ce1-2a54-4ff4-a660-14629a3df69f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 43074-108-01 | 43074010801 | 3 mL in 1 BOTTLE, DROPPER | 3 ml | Historical |
| 43074-108-02 | 43074010802 | 1 in 1 BOTTLE, PLASTIC | | Historical |