Doxycycline Hyclate
- Product NDC
- 72789-419
- 11-digit product format
- 727890419
- Labeler code
- 72789
- Product ID
- 72789-419_383ebab1-4b2e-be4e-e063-6294a90a7d2e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline Hyclate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA062677
- Marketing category
- ANDA
- Marketing start
- 1986-07-10
- 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 |
|---|
| 72789-419-14 | Doxycycline Hyclate | 14 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 14 | | 24 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72789-419 | DOXYCYCLINE HYCLATE TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.] | 23 | Current NDC, 1 package rows | 20250221_cf95b2ca-2cf8-49a8-8e3a-f9b0f5b2072c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72789-419-14 | 72789041914 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-419-14) | 2024-07-03 | No | No | Current |