Doxycycline Hyclate
- Product NDC
- 62135-623
- 11-digit product format
- 621350623
- Labeler code
- 62135
- Product ID
- 62135-623_32d032a2-c17d-4b61-e063-6394a90a9a95
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline Hyclate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Chartwell RX, LLC
- Application
- ANDA065277
- Marketing category
- ANDA
- Marketing start
- 2005-11-10
- Substance
- DOXYCYCLINE HYCLATE
- Active strength
- 20 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 | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 19XTS3T51U |
| Rxcui | 283535 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62135-623-90 | Doxycycline Hyclate | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62135-623 | DOXYCYCLINE HYCLATE TABLET, FILM COATED [CHARTWELL RX, LLC] | 2 | Current NDC, 1 package rows | 20250417_b3294889-e8f8-42f1-9bd0-13d87572997a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 62135-623-90 | 62135062390 | 90 TABLET, FILM COATED in 1 BOTTLE (62135-623-90) | 2023-02-20 | No | No | Current |