Cromolyn Sodium
- Product NDC
- 71205-085
- 11-digit product format
- 712050085
- Labeler code
- 71205
- Product ID
- 71205-085_0b4a28ff-6e7e-45ee-a11c-98dd4127b2fb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cromolyn Sodium
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Proficient Rx LP
- Application
- ANDA074706
- Marketing category
- ANDA
- Marketing start
- 1998-04-29
- Marketing end
- 0000-00-00
- Substance
- CROMOLYN SODIUM
- Active strength
- 40 mg/mL
- Pharmacologic classes
- Decreased Histamine Release [PE],Mast Cell Stabilizer [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-085 | CROMOLYN SODIUM SOLUTION/ DROPS [PROFICIENT RX LP] | 3 | Legacy NDC | 20191029_9616c0b9-c22a-4b0a-b379-376fa51beb05.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-085-10 | 71205008510 | 1 BOTTLE, DROPPER in 1 CARTON (71205-085-10) > 10 mL in 1 BOTTLE, DROPPER | 2018-08-01 | 0000-00-00 | No | No | Current |