Doxycycline Hyclate
- Product NDC
- 71610-117
- 11-digit product format
- 716100117
- Labeler code
- 71610
- Product ID
- 71610-117_610243f6-9761-4cdf-ad1a-0cb65c3d4445
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline Hyclate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA062505
- Marketing category
- ANDA
- Marketing start
- 1984-09-11
- Marketing end
- 0000-00-00
- Substance
- DOXYCYCLINE HYCLATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC],Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 71610-117 | DOXYCYCLINE HYCLATE TABLET, FILM COATED [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC] | 1 | Legacy NDC | 20181102_fa24a981-ea4c-41af-bd1e-4af039bcf767.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71610-117-30 | 71610011730 | 30 TABLET, FILM COATED in 1 BOTTLE (71610-117-30) | 2018-09-06 | 0000-00-00 | No | No | Current |