Doxycycline Hyclate
- Product NDC
- 55695-032
- 11-digit product format
- 556950032
- Labeler code
- 55695
- Product ID
- 55695-032_2b5a2794-49ce-6a30-e054-00144ff88e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline Hyclate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Department of State Health Services, Pharmacy Branch
- Application
- ANDA062677
- Marketing category
- ANDA
- Marketing start
- 1986-07-10
- Marketing end
- 0000-00-00
- Substance
- DOXYCYCLINE HYCLATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC],Tetracyclines [CS]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 55695-032-00 | Doxycycline Hyclate | 500 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 500 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55695-032 | DOXYCYCLINE HYCLATE TABLET, FILM COATED [DEPARTMENT OF STATE HEALTH SERVICES, PHARMACY BRANCH] | 1 | Legacy NDC, 1 package rows | 20160311_2b5a2794-49cd-6a30-e054-00144ff88e88.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 55695-032-00 | 55695003200 | 500 in 1 BOTTLE, PLASTIC | Historical |