Doxycycline Hyclate
- Product NDC
- 42708-173
- 11-digit product format
- 427080173
- Labeler code
- 42708
- Product ID
- 42708-173_46827da0-577c-60e7-e063-6294a90a99e7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline Hyclate
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- QPharma, Inc.
- Application
- ANDA065095
- Marketing category
- ANDA
- Marketing start
- 2003-07-02
- Substance
- DOXYCYCLINE HYCLATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC], Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Doxycycline Hyclate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DOXYCYCLINE HYCLATE | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 19XTS3T51U |
| Rxcui | 1650143 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 42708-173-20 | Doxycycline Hyclate | 20 in 1 BOTTLE, PLASTIC | TABLET, COATED | 20 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42708-173 | DOXYCYCLINE HYCLATE TABLET, COATED [QPHARMA, INC.] | 5 | Current NDC, 1 package rows | 20250522_fbd0a22f-b365-c0a2-e053-6394a90a1e07.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 42708-173-20 | 42708017320 | 20 TABLET, COATED in 1 BOTTLE, PLASTIC (42708-173-20) | 2023-05-19 | Yes | No | Historical |