Prescription drug · ANDA
Doxycycline NDC 70771-1007
Doxycycline 75 mg/1 · Tablet, Film coated · Oral · Zydus Lifesciences Limited
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70771-1007-1 | 70771100701 | 100 TABLET, FILM COATED in 1 BOTTLE (70771-1007-1)Marketed from Jan 11, 2018 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Doxycycline
- Generic name (nonproprietary)
- doxycycline
- Active ingredients
- Doxycycline — 75 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Zydus Lifesciences Limited
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 209582
- Marketing start
- Listing expires
- Other FDA classes
- Tetracyclines (Chemical structure)
- Identifiers
- Product ID 70771-1007_1f788250-9643-4c64-bb4e-4dfefabb8c01SPL ID 1f788250-9643-4c64-bb4e-4dfefabb8c01SPL set ID c886b2e4-494a-4325-abaf-981fc3d01c66RxCUI 1649429, 1650142, 1650444, 1652673UNII N12000U13OUPC 0370710112431
- Pharmacologic class
- Tetracycline-class Drug
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N470771100701followed by a unit qualifier and the quantityPackage 70771-1007-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Label details couldn’t be retrieved right now. Open the label on DailyMed.
Other NDCs under ANDA 209582
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Doxycycline | Doxycycline 50 mg/1 | Tablet, Film coatedOral | Zydus Pharmaceuticals USA Inc. | 70710-1121 |
| Doxycycline | Doxycycline 150 mg/1 | Tablet, Film coatedOral | Zydus Pharmaceuticals USA Inc. | 70710-1124 |
| Doxycycline | Doxycycline 75 mg/1 | Tablet, Film coatedOral | Zydus Pharmaceuticals USA Inc. | 70710-1122 |
| Doxycycline | Doxycycline 100 mg/1 | Tablet, Film coatedOral | Zydus Pharmaceuticals USA Inc. | 70710-1123 |
| Doxycycline | Doxycycline 100 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-2638 |
| Doxycycline Monohydrate | Doxycycline 100 mg/1 | Tablet, Film coatedOral | Advanced Rx Pharmacy of Tennessee, LLC | 80425-0319 |
| Doxycycline | Doxycycline 100 mg/1 | Tablet, Film coatedOral | Proficient Rx LP | 82804-028 |
| Doxycycline | Doxycycline 100 mg/1 | Tablet, Film coatedOral | A-S Medication Solutions | 50090-3809 |
| Doxycycline | Doxycycline 50 mg/1 | Tablet, Film coatedOral | Zydus Lifesciences Limited | 70771-1006 |
| Doxycycline | Doxycycline 100 mg/1 | Tablet, Film coatedOral | Zydus Lifesciences Limited | 70771-1008 |
| Doxycycline | Doxycycline 150 mg/1 | Tablet, Film coatedOral | Zydus Lifesciences Limited | 70771-1009 |