Uline Antacid
- Product NDC
- 69790-089
- 11-digit product format
- 697900089
- Labeler code
- 69790
- Product ID
- 69790-089_debc3184-6bb1-11d1-e053-2995a90af277
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- calcium carbonate
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- Uline
- Application
- part331
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2019-10-07
- Marketing end
- 0000-00-00
- Substance
- CALCIUM CARBONATE
- Active strength
- 420 mg/1
- Pharmacologic classes
- Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69790-089-33 | Uline Antacid | 2 in 1 PACKET | TABLET, CHEWABLE | 2 | | 9 |
| 69790-089-33 | Uline Antacid | 50 in 1 BOX | TABLET, CHEWABLE | 50 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69790-089 | ULINE ANTACID (CALCIUM CARBONATE) TABLET, CHEWABLE [ULINE] | 8 | Legacy NDC, 2 package rows | 20240127_9014f295-e816-9bcd-e053-2a95a90ae103.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69790-089-33 | 69790008933 | 50 PACKET in 1 BOX (69790-089-33) > 2 TABLET, CHEWABLE in 1 PACKET | 50 packet | 2019-10-07 | 0000-00-00 | No | No | Current |