DOXYCYCLINE HYCLATE
- Product NDC
- 71335-2639
- 11-digit product format
- 713352639
- Labeler code
- 71335
- Product ID
- 71335-2639_60a530a7-5529-4ce2-8dc2-c5ecb8615ba9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DOXYCYCLINE HYCLATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA211343
- Marketing category
- ANDA
- Marketing start
- 2019-10-09
- Substance
- DOXYCYCLINE HYCLATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC], Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- DOXYCYCLINE HYCLATE
- Listing expiration
- 2027-12-31
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 |
|---|
| 71335-2639-1 | DOXYCYCLINE HYCLATE | 14 in 1 BOTTLE | TABLET | 14 | | 100 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2639-1 | 71335263901 | 14 TABLET in 1 BOTTLE (71335-2639-1) | 14 tablet | 2026-04-13 | No | No | Current |