Diclofenac Sodium
- Product NDC
- 71335-0138
- 11-digit product format
- 713350138
- Labeler code
- 71335
- Product ID
- 71335-0138_848a92eb-e434-48df-bc65-0c7a5a7779c5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074394
- Marketing category
- ANDA
- Marketing start
- 1995-11-30
- Marketing end
- 0000-00-00
- Substance
- DICLOFENAC SODIUM
- Active strength
- 75 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 71335-0138-0 | EA - Each | 71335-0138 | 8f9fa09a-b1d6-4222-8900-5aa2501e553e | 1 | 2018-03-08 |
| 71335-0138-1 | EA - Each | 71335-0138 | 96aacb23-c690-431b-943f-9efc392e7cb8 | 1 | 2018-03-08 |
| 71335-0138-2 | EA - Each | 71335-0138 | 0de7202b-0acf-4966-b273-db2a7074d618 | 1 | 2018-03-08 |
| 71335-0138-3 | EA - Each | 71335-0138 | 7ae77d76-71dd-43e5-94d6-7f9be813a3b7 | 1 | 2018-03-08 |
| 71335-0138-4 | EA - Each | 71335-0138 | a093eaab-3dd2-4c21-9943-5640f2d476d8 | 1 | 2018-03-08 |
| 71335-0138-5 | EA - Each | 71335-0138 | a8cf0dcc-bb95-4018-9ad6-b664f36b9ba9 | 1 | 2018-03-08 |
| 71335-0138-6 | EA - Each | 71335-0138 | 810f9719-b8e7-488b-91c3-9ab644e0f39f | 1 | 2018-03-08 |
| 71335-0138-7 | EA - Each | 71335-0138 | 8342a4e2-d9a3-4c87-b2de-267916502180 | 1 | 2018-03-08 |
| 71335-0138-8 | EA - Each | 71335-0138 | 3c48dfd3-b3b8-44b4-b622-14aeed5f4287 | 1 | 2018-03-08 |
| 71335-0138-9 | EA - Each | 71335-0138 | 33c884c3-fbde-4506-a58e-f78a63c696cc | 1 | 2018-03-08 |